This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v1.0.0: STU 1) based on FHIR R4. The current version which supercedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions

Human Genome Variation Society Sequence Variant Nomenclature Value Set - XML Representation

(back to description)

Raw xml

Source view

<ValueSet xmlns="http://hl7.org/fhir">
  <id value="mcode-hgvs-vs"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><h2>Human Genome Variation Society Sequence Variant Nomenclature Value Set</h2><div><p>HGVS nomenclature is used to report and exchange information regarding variants found in DNA, RNA, and protein sequences.</p>
</div><ul><li>Include all codes defined in <code>http://varnomen.hgvs.org</code></li></ul></div>
  </text>
  <url value="http://hl7.org/fhir/us/mcode/ValueSet/mcode-hgvs-vs"/>
  <version value="1.0.0"/>
  <name value="HGVSVS"/>
  <title
         value="Human Genome Variation Society Sequence Variant Nomenclature Value Set"/>
  <status value="active"/>
  <date value="2020-03-18T15:32:10+00:00"/>
  <publisher value="HL7 International Clinical Interoperability Council"/>
  <contact>
    <name value="HL7 International Clinical Interoperability Council"/>
    <telecom>
      <system value="url"/>
      <value value="http://www.hl7.org/Special/committees/cic"/>
    </telecom>
    <telecom>
      <system value="email"/>
      <value value="ciclist@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."/>
  <compose>
    <include>
      <system value="http://varnomen.hgvs.org"/>
    </include>
  </compose>
</ValueSet>