Canonical Allele Identifier: CA211676950

Gene: CYP2C19

Linked Data

• dbSNP Id: rs143075956
• gnomAD v4: 10-94775154-G-C
• MyVariant Identifiers: chr10:g.96534911G>C (hg19) ; chr10:g.94775154G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775154G>C , CM000672.2:g.94775154G>C	GRCh38
NC_000010.10:g.96534911G>C , CM000672.1:g.96534911G>C	GRCh37
NC_000010.9:g.96524901G>C	NCBI36
NG_008384.2:g.17449G>C
NG_008384.3:g.17474G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.265G>C MANE Select	ENSP00000360372.3:p.Asp89His
ENST00000645461.1:n.1318G>C
ENST00000371321.7:c.265G>C	ENSP00000360372.3:p.Asp89His
ENST00000464755.1:c.1028G>C	ENSP00000483243.1:n.1028G>C
ENST00000480405.2:c.265G>C	ENSP00000483847.1:p.Asp89His
NM_000769.2:c.265G>C	NP_000760.1:p.Asp89His
NM_000769.4:c.265G>C MANE Select	NP_000760.1:p.Asp89His