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 (HL7® FHIR® Standard) R4. The current version which supersedes this version is 4.0.0. 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"
}
]
}
}