c1cd528300bee12948fd6645afee65cbc789926b
max
  Mon Nov 6 11:58:41 2023 -0800
docing ID:start-end a feature that was only remembered by Hiram's neurons

diff --git src/hg/htdocs/goldenPath/help/query.html src/hg/htdocs/goldenPath/help/query.html
index 5675931..83cab8e 100755
--- src/hg/htdocs/goldenPath/help/query.html
+++ src/hg/htdocs/goldenPath/help/query.html
@@ -118,30 +118,33 @@
     <td>NP_059110</td>
     <td>Displays the region containing protein accession number NP_059110</td></tr> 
   <tr>
     <td>PRNP</td>
     <td>Displays the region containing HUGO Gene Nomenclature Committee identifier PRNP</td></tr> 
   <tr>
   <tr>
     <td>Q99697</td>
     <td>Displays the region containing the alignment of the UniProt/SwissProt protein sequence with accession Q99697 (PITX2)</td></tr> 
   <tr>
     <td nowrap>RH18061;RH80175<br>15q11;15q13<br>NM_012090.5;NM_012421.4</td>
     <td nowrap>Displays the region between genome landmarks, such as the STS markers RH18061 and 
     RH80175, or chromosome<br> bands 15q11 to 15q13, or SNPs NM_000310.4 and NM_012090.5. This syntax
     may also be used for other range queries,<br>such as between uniquely determined ESTs, mRNAs, 
     refSeqs, SNPS, etc.</td></tr>
+  <tr>
+    <td>NR_026861.1:1-1000</td>
+    <td>Works with any other type of accession from this page: Displays the first 1000bp of NR_026861.1</td></tr> 
   <tr id="HGVS">
     <td nowrap>NM_000310.4(PPT1):c.271_287del17insTT<br> NM_007262.5(PARK7):c.-24+75_-24+92dup<br>
     NM_006172.4(NPPA):c.456_*1delAA<br> MYH11:c.503-14_503-12del<br> 
     NM_198576.4(AGRN):c.1057C&gt;T<br> NM_198056.3:c.1654G&gt;T<br> NP_002993.1:p.Asp92Glu<br>
     NP_002993.1:p.D92E<br> BRCA1 Ala744Cys<br> BRCA1 A744C<br> LRG_100t1:c.4G>A<br> LRG_100t1:n.1<br>
     LRG_456p1:p.Ser190Leu<br>LRG_321:g.16409_16461del<br>ENST00000002596.6:c.-108-6848A&gt;G<br>
     ENSP00000005178.5:p.Val20Gly<br>
     chrX:g.31500000_31600000del<br> NR_111987:n.-1 <br> NM_015102.5:n.3038-2<br>
     NM_001372044:c.1528_1530del</td>
     <td>Displays the region that matches the <a href="http://varnomen.hgvs.org/" target="_blank">HGVS</a> 
         expression, usually in the format <tt>&lt;transcript or protein&gt;:&lt;position&gt; &lt;amino acid or nucleotide change&gt;</tt><br>If a gene symbol is used, HGVS search will try all RefSeq transcripts to find the nucleotide or amino acid at the position indicated in the expression. If there are multiple matches, a disambiguation page will be shown. If the RefSeq sequence differs from the genome sequence, then currently the search will use the genome, not the transcript, for codon counting and amino acid / nucleotide  comparison. Please contact us if this is inconvenient.</td></tr> 
 <!-- commented out -- not working 
   <tr> 
     <td>15q11;15q13</td>
     <td>bands 15q11 to 15q13, or SNPs rs1042522 and rs1800370. This syntax may also be used for