Canonical Allele Identifier: CA1929218767

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775423A= , CM000672.2:g.94775423A=	GRCh38
NC_000010.10:g.96535180A= , CM000672.1:g.96535180A=	GRCh37
NC_000010.9:g.96525170A=	NCBI36
NG_008384.2:g.17718A=
NG_008384.3:g.17743A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.365A= MANE Select	ENSP00000360372.3:p.Glu122=
ENST00000645461.1:n.1418A=
ENST00000371321.7:c.365A=	ENSP00000360372.3:p.Glu122=
ENST00000464755.1:c.1128A=	ENSP00000483243.1:n.1128A=
ENST00000480405.2:c.365A=	ENSP00000483847.1:p.Glu122=
NM_000769.2:c.365A=	NP_000760.1:p.Glu122=
NM_000769.4:c.365A= MANE Select	NP_000760.1:p.Glu122=