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