Canonical Allele Identifier: CA595638641

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1268591206
• gnomAD v2: 10-96535012-T-C
• gnomAD v4: 10-94775255-T-C
• MyVariant Identifiers: chr10:g.96535012T>C (hg19) ; chr10:g.94775255T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775255T>C , CM000672.2:g.94775255T>C	GRCh38
NC_000010.10:g.96535012T>C , CM000672.1:g.96535012T>C	GRCh37
NC_000010.9:g.96525002T>C	NCBI36
NG_008384.2:g.17550T>C
NG_008384.3:g.17575T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.331+35T>C MANE Select	ENSP00000360372.3:n.331+35T>C
ENST00000645461.1:n.1384+35T>C
ENST00000371321.7:c.331+35T>C	ENSP00000360372.3:n.331+35T>C
ENST00000464755.1:c.1094+35T>C	ENSP00000483243.1:n.1094+35T>C
ENST00000480405.2:c.331+35T>C	ENSP00000483847.1:n.331+35T>C
NM_000769.2:c.331+35T>C	NP_000760.1:n.331+35T>C
NM_000769.4:c.331+35T>C MANE Select	NP_000760.1:n.331+35T>C