Canonical Allele Identifier: CA1929221619

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780609A= , CM000672.2:g.94780609A=	GRCh38
NC_000010.10:g.96540366A= , CM000672.1:g.96540366A=	GRCh37
NC_000010.9:g.96530356A=	NCBI36
NG_008384.2:g.22904A=
NG_008384.3:g.22929A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.592A= MANE Select	ENSP00000360372.3:p.Met198=
ENST00000645461.1:n.1645A=
ENST00000371321.7:c.592A=	ENSP00000360372.3:p.Met198=
ENST00000464755.1:c.1355A=	ENSP00000483243.1:n.1355A=
NM_000769.2:c.592A=	NP_000760.1:p.Met198=
NM_000769.4:c.592A= MANE Select	NP_000760.1:p.Met198=