Canonical Allele Identifier: CA211697124
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs17882796
gnomAD v2: 10-96612753-T-C
gnomAD v3: 10-94852996-T-C
gnomAD v4: 10-94852996-T-C
MyVariant Identifiers: chr10:g.96612753T>C (hg19) chr10:g.94852996T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852996T>C , CM000672.2:g.94852996T>C GRCh38
NC_000010.10:g.96612753T>C , CM000672.1:g.96612753T>C GRCh37
NC_000010.9:g.96602743T>C NCBI36
NG_008384.2:g.95291T>C
NG_008384.3:g.95316T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*82T>C MANE Select ENSP00000360372.3:n.*82T>C
ENST00000645461.1:n.2466T>C
ENST00000371321.7:c.*82T>C ENSP00000360372.3:n.*82T>C
ENST00000464755.1:c.2318T>C ENSP00000483243.1:n.2318T>C
NM_000769.2:c.*82T>C NP_000760.1:n.*82T>C
NM_000769.4:c.*82T>C MANE Select NP_000760.1:n.*82T>C
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