Canonical Allele Identifier: CA5616828

Gene: CYP2C19

Linked Data

• dbSNP Id: rs778831562
• ExAC: 10:96612474 T / A
• gnomAD v2: 10-96612474-T-A
• gnomAD v4: 10-94852717-T-A
• MyVariant Identifiers: chr10:g.96612474T>A (hg19) ; chr10:g.94852717T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852717T>A , CM000672.2:g.94852717T>A	GRCh38
NC_000010.10:g.96612474T>A , CM000672.1:g.96612474T>A	GRCh37
NC_000010.9:g.96602464T>A	NCBI36
NG_008384.2:g.95012T>A
NG_008384.3:g.95037T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1292-16T>A MANE Select	ENSP00000360372.3:n.1292-16T>A
ENST00000645461.1:n.2203-16T>A
ENST00000371321.7:c.1292-16T>A	ENSP00000360372.3:n.1292-16T>A
ENST00000464755.1:c.2055-16T>A	ENSP00000483243.1:n.2055-16T>A
NM_000769.2:c.1292-16T>A	NP_000760.1:n.1292-16T>A
NM_000769.4:c.1292-16T>A MANE Select	NP_000760.1:n.1292-16T>A