{
  "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/3.0.0/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": "2.0.0",
  "name": "HGVSVS",
  "title": "Human Genome Variation Society Sequence Variant Nomenclature Value Set",
  "status": "active",
  "date": "2022-01-18T03:17:40+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"
      }
    ]
  }
}