Canonical Allele Identifier: CA1929218799

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775468G= , CM000672.2:g.94775468G=	GRCh38
NC_000010.10:g.96535225G= , CM000672.1:g.96535225G=	GRCh37
NC_000010.9:g.96525215G=	NCBI36
NG_008384.2:g.17763G=
NG_008384.3:g.17788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.410G= MANE Select	ENSP00000360372.3:p.Gly137=
ENST00000645461.1:n.1463G=
ENST00000371321.7:c.410G=	ENSP00000360372.3:p.Gly137=
ENST00000464755.1:c.1173G=	ENSP00000483243.1:n.1173G=
ENST00000480405.2:c.410G=	ENSP00000483847.1:p.Gly137=
NM_000769.2:c.410G=	NP_000760.1:p.Gly137=
NM_000769.4:c.410G= MANE Select	NP_000760.1:p.Gly137=