minimal Common Oncology Data Elements (mCODE) Implementation Guide
1.16.0 - STU Release 2 (Ballot Version)

This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v1.16.0: STU 2 Ballot 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 - JSON Representation

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{
  "resourceType" : "ValueSet",
  "id" : "mcode-hgvs-vs",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include all codes defined in <a href=\"https://terminology.hl7.org/1.0.0//CodeSystem-v3-hgvs.html\"><code>http://varnomen.hgvs.org</code></a></li></ul></div>"
  },
  "url" : "http://hl7.org/fhir/us/mcode/ValueSet/mcode-hgvs-vs",
  "version" : "1.16.0",
  "name" : "HGVSVS",
  "title" : "Human Genome Variation Society Sequence Variant Nomenclature Value Set",
  "status" : "active",
  "date" : "2021-04-15T12:44:45+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.",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "urn:iso:std:iso:3166",
          "code" : "US",
          "display" : "United States of America"
        }
      ]
    }
  ],
  "compose" : {
    "include" : [
      {
        "system" : "http://varnomen.hgvs.org"
      }
    ]
  }
}