Canonical Allele Identifier: CA1929218601

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775133G= , CM000672.2:g.94775133G=	GRCh38
NC_000010.10:g.96534890G= , CM000672.1:g.96534890G=	GRCh37
NC_000010.9:g.96524880G=	NCBI36
NG_008384.2:g.17428G=
NG_008384.3:g.17453G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.244G= MANE Select	ENSP00000360372.3:p.Val82=
ENST00000645461.1:n.1297G=
ENST00000371321.7:c.244G=	ENSP00000360372.3:p.Val82=
ENST00000464755.1:c.1007G=	ENSP00000483243.1:n.1007G=
ENST00000480405.2:c.244G=	ENSP00000483847.1:p.Val82=
NM_000769.2:c.244G=	NP_000760.1:p.Val82=
NM_000769.4:c.244G= MANE Select	NP_000760.1:p.Val82=