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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.
The Human Genome Variation Society maintains the recommendations for describing sequence variants (Wikipedia; the current rules are at hgvs-nomenclature.org). A description names the reference sequence and level (g. genomic, c. coding DNA, p. protein) and the change, and a genomic description depends on the genome build. Free-text variant names in papers (L858R, T790M) are shorthand for HGVS protein descriptions; joining them to databases such as ClinVar and CIViC requires the full form.
Shares Genome builds: GRCh38 versus hg19 (GRCh37), Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Genome builds: GRCh38 versus hg19 (GRCh37), Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Variant calling, Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Genome builds: GRCh38 versus hg19 (GRCh37), Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Variant calling, Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Variant effect prediction, Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Variant effect prediction, Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Variant effect prediction, Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.