Canonical Allele Identifier: CA1929218903

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775649G= , CM000672.2:g.94775649G=	GRCh38
NC_000010.10:g.96535406G= , CM000672.1:g.96535406G=	GRCh37
NC_000010.9:g.96525396G=	NCBI36
NG_008384.2:g.17944G=
NG_008384.3:g.17969G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.481+110G= MANE Select	ENSP00000360372.3:n.481+110G=
ENST00000645461.1:n.1534+110G=
ENST00000371321.7:c.481+110G=	ENSP00000360372.3:n.481+110G=
ENST00000464755.1:c.1244+110G=	ENSP00000483243.1:n.1244+110G=
ENST00000480405.2:c.*102G=	ENSP00000483847.1:n.*102G=
NM_000769.2:c.481+110G=	NP_000760.1:n.481+110G=
NM_000769.4:c.481+110G= MANE Select	NP_000760.1:n.481+110G=