Canonical Allele Identifier: CA1929278468

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850281C= , CM000672.2:g.94850281C=	GRCh38
NC_000010.10:g.96610038C= , CM000672.1:g.96610038C=	GRCh37
NC_000010.9:g.96600028C=	NCBI36
NG_008384.2:g.92576C=
NG_008384.3:g.92601C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1291+223C= MANE Select	ENSP00000360372.3:n.1291+223C=
ENST00000645461.1:n.2202+223C=
ENST00000371321.7:c.1291+223C=	ENSP00000360372.3:n.1291+223C=
ENST00000464755.1:c.2054+223C=	ENSP00000483243.1:n.2054+223C=
NM_000769.2:c.1291+223C=	NP_000760.1:n.1291+223C=
NM_000769.4:c.1291+223C= MANE Select	NP_000760.1:n.1291+223C=