# OnCo record hgvs (term). Data CC BY-NC 4.0, attribute "Data from OnCo (onco.cc)". Whole corpus: https://onco.cc/api/v1/onco.nt
@prefix schema: <https://schema.org/> .
@prefix onco: <https://onco.cc/ns#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

<https://onco.cc/terms/hgvs/>
  a schema:DefinedTerm ;
  onco:kind "term" ;
  schema:identifier "hgvs" ;
  schema:name "HGVS variant nomenclature"@en ;
  schema:alternateName "HGVS"@en, "HGVS nomenclature"@en, "HGVS notation"@en, "c. notation"@en, "p. notation"@en, "variant nomenclature"@en ;
  schema:description "HGVS is the standard way to write a DNA or protein change, such as EGFR c.2573T>G or p.Leu858Arg, so that the same variant is named the same way everywhere."@en ;
  schema:url <https://onco.cc/terms/hgvs/> ;
  schema:dateModified "2026-09-24"^^xsd:date ;
  schema:sameAs <https://en.wikipedia.org/wiki/Human_Genome_Variation_Society> ;
  schema:citation <https://hgvs-nomenclature.org/stable/>, <https://en.wikipedia.org/wiki/Human_Genome_Variation_Society> ;
  onco:tag "cansim-terms" ;
  onco:related <https://onco.cc/collections/clinvar/>, <https://onco.cc/collections/civic/>, <https://onco.cc/terms/cancer-ai-vocabulary/> ;
  onco:terms <https://onco.cc/terms/genome-builds/>, <https://onco.cc/terms/variant-effect-prediction/>, <https://onco.cc/terms/variant-calling/> .