Genomics Reporting Implementation Guide
2.0.0 - trial-use

This page is part of the Genetic Reporting Implementation Guide (v2.0.0: STU 2) based on FHIR R4. This is the current published version. For a full list of available versions, see the Directory of published versions

: Human Genome Variation Society (HGVS) Nomenclature - JSON Representation

Raw json | Download


{
  "resourceType" : "ValueSet",
  "id" : "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/3.1.0/CodeSystem-v3-hgvs.html\"><code>http://varnomen.hgvs.org</code></a></li></ul></div>"
  },
  "url" : "http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs",
  "version" : "2.0.0",
  "name" : "HGVSVS",
  "title" : "Human Genome Variation Society (HGVS) Nomenclature",
  "status" : "active",
  "date" : "2022-05-09T16:59:16+00:00",
  "publisher" : "HL7 Clinical Genomics Working Group",
  "contact" : [
    {
      "name" : "HL7 Clinical Genomics Working Group",
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://www.hl7.org/Special/committees/clingenomics"
        },
        {
          "system" : "email",
          "value" : "cg@lists.HL7.org"
        }
      ]
    }
  ],
  "description" : "HGVS-nomenclature is used to report and exchange information regarding variants found in DNA, RNA and protein sequences and serves as an international standard. (source: varnomen.hgvs.org)",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code" : "001",
          "display" : "World"
        }
      ]
    }
  ],
  "compose" : {
    "include" : [
      {
        "system" : "http://varnomen.hgvs.org"
      }
    ]
  }
}