{
  "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=\"http://terminology.hl7.org/5.0.0/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" : "2.1.0",
  "name" : "HGVSVS",
  "title" : "Human Genome Variation Society Sequence Variant Nomenclature Value Set",
  "status" : "active",
  "experimental" : false,
  "date" : "2023-03-21T04:54:56+11:00",
  "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"
    }]
  }
}