This page is part of the Genetic Reporting Implementation Guide (v3.0.0: STU3) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions
Active as of 2024-12-12 |
<ValueSet xmlns="http://hl7.org/fhir">
<id value="hgvs-vs"/>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: ValueSet hgvs-vs</b></p><a name="hgvs-vs"> </a><a name="hchgvs-vs"> </a><a name="hgvs-vs-en-US"> </a><ul><li>Include all codes defined in <a href="http://terminology.hl7.org/6.1.0/CodeSystem-v3-hgvs.html"><code>http://varnomen.hgvs.org</code></a></li></ul></div>
</text>
<extension
url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg">
<valueCode value="cg"/>
</extension>
<url value="http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs"/>
<version value="3.0.0"/>
<name value="HGVSVS"/>
<title value="Human Genome Variation Society (HGVS) Nomenclature"/>
<status value="active"/>
<experimental value="false"/>
<date value="2024-12-12T21:16:09+00:00"/>
<publisher value="HL7 International / Clinical Genomics"/>
<contact>
<name value="HL7 International / Clinical Genomics"/>
<telecom>
<system value="url"/>
<value value="http://www.hl7.org/Special/committees/clingenomics"/>
</telecom>
<telecom>
<system value="email"/>
<value value="cg@lists.HL7.org"/>
</telecom>
</contact>
<description
value="HGVS-nomenclature is used to report and exchange information regarding variants found in DNA, RNA and protein sequences and serves as an international standard. (source: varnomen.hgvs.org)"/>
<jurisdiction>
<coding>
<system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/>
<code value="001"/>
<display value="World"/>
</coding>
</jurisdiction>
<compose>
<include>
<system value="http://varnomen.hgvs.org"/>
</include>
</compose>
</ValueSet>