Canonical Allele Identifier: CA1929221685

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780729T= , CM000672.2:g.94780729T=	GRCh38
NC_000010.10:g.96540486T= , CM000672.1:g.96540486T=	GRCh37
NC_000010.9:g.96530476T=	NCBI36
NG_008384.2:g.23024T=
NG_008384.3:g.23049T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.642+70T= MANE Select	ENSP00000360372.3:n.642+70T=
ENST00000645461.1:n.1695+70T=
ENST00000371321.7:c.642+70T=	ENSP00000360372.3:n.642+70T=
ENST00000464755.1:c.1405+70T=	ENSP00000483243.1:n.1405+70T=
NM_000769.2:c.642+70T=	NP_000760.1:n.642+70T=
NM_000769.4:c.642+70T= MANE Select	NP_000760.1:n.642+70T=