{
  "package" : "hl7.terminology.r4@6.3.0",
  "definition" : "Locus Reference Genomic (LRG)",
  "system" : "http://terminology.hl7.org/CodeSystem/v2-0396",
  "property" : [ {
    "_uri" : "http://terminology.hl7.org/CodeSystem/utg-concept-properties#v2-concComment",
    "code" : "v2-concComment",
    "valueString" : "LRG is a manually curated record that contains stable and thus, un-versioned reference sequences designed specifically for reporting sequence variants with clinical implications. \nIt provides a genomic DNA sequence representation of a single gene that is idealized, has a permanent ID (with no versioning), and core content that never changes. Their database includes maps to NCBI, Ensembl and USCS reference sequences."
  }, {
    "_uri" : "http://terminology.hl7.org/CodeSystem/utg-concept-properties#status",
    "code" : "status",
    "valueCode" : "A"
  } ],
  "codesystem" : "e39b54bc-250f-5dcb-bad5-a06bddcbf336",
  "concept_id" : "a304cef5-788e-5dbe-bf0d-816f89117155",
  "ancestors" : {
    "LRG-RefSeq" : 0
  },
  "id" : "5214691c-b4d0-42e6-a192-283e72704c24",
  "code" : "LRG-RefSeq",
  "display" : "Locus Reference Genomic (LRG)",
  "version" : "4.1.0"
}