Canonical Allele Identifier: CA211677622

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1027055692
• gnomAD v3: 10-94775777-T-C
• gnomAD v4: 10-94775777-T-C
• MyVariant Identifiers: chr10:g.96535534T>C (hg19) ; chr10:g.94775777T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775777T>C , CM000672.2:g.94775777T>C	GRCh38
NC_000010.10:g.96535534T>C , CM000672.1:g.96535534T>C	GRCh37
NC_000010.9:g.96525524T>C	NCBI36
NG_008384.2:g.18072T>C
NG_008384.3:g.18097T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.481+238T>C MANE Select	ENSP00000360372.3:n.481+238T>C
ENST00000645461.1:n.1534+238T>C
ENST00000371321.7:c.481+238T>C	ENSP00000360372.3:n.481+238T>C
ENST00000464755.1:c.1244+238T>C	ENSP00000483243.1:n.1244+238T>C
ENST00000480405.2:c.*230T>C	ENSP00000483847.1:n.*230T>C
NM_000769.2:c.481+238T>C	NP_000760.1:n.481+238T>C
NM_000769.4:c.481+238T>C MANE Select	NP_000760.1:n.481+238T>C