Canonical Allele Identifier: CA1929218617

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775166G= , CM000672.2:g.94775166G=	GRCh38
NC_000010.10:g.96534923G= , CM000672.1:g.96534923G=	GRCh37
NC_000010.9:g.96524913G=	NCBI36
NG_008384.2:g.17461G=
NG_008384.3:g.17486G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.277G= MANE Select	ENSP00000360372.3:p.Glu93=
ENST00000645461.1:n.1330G=
ENST00000371321.7:c.277G=	ENSP00000360372.3:p.Glu93=
ENST00000464755.1:c.1040G=	ENSP00000483243.1:n.1040G=
ENST00000480405.2:c.277G=	ENSP00000483847.1:p.Glu93=
NM_000769.2:c.277G=	NP_000760.1:p.Glu93=
NM_000769.4:c.277G= MANE Select	NP_000760.1:p.Glu93=