Canonical Allele Identifier: CA1929278369

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850136C= , CM000672.2:g.94850136C=	GRCh38
NC_000010.10:g.96609893C= , CM000672.1:g.96609893C=	GRCh37
NC_000010.9:g.96599883C=	NCBI36
NG_008384.2:g.92431C=
NG_008384.3:g.92456C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1291+78C= MANE Select	ENSP00000360372.3:n.1291+78C=
ENST00000645461.1:n.2202+78C=
ENST00000371321.7:c.1291+78C=	ENSP00000360372.3:n.1291+78C=
ENST00000464755.1:c.2054+78C=	ENSP00000483243.1:n.2054+78C=
NM_000769.2:c.1291+78C=	NP_000760.1:n.1291+78C=
NM_000769.4:c.1291+78C= MANE Select	NP_000760.1:n.1291+78C=