Canonical Allele Identifier: CA1929221691

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780739G= , CM000672.2:g.94780739G=	GRCh38
NC_000010.10:g.96540496G= , CM000672.1:g.96540496G=	GRCh37
NC_000010.9:g.96530486G=	NCBI36
NG_008384.2:g.23034G=
NG_008384.3:g.23059G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.642+80G= MANE Select	ENSP00000360372.3:n.642+80G=
ENST00000645461.1:n.1695+80G=
ENST00000371321.7:c.642+80G=	ENSP00000360372.3:n.642+80G=
ENST00000464755.1:c.1405+80G=	ENSP00000483243.1:n.1405+80G=
NM_000769.2:c.642+80G=	NP_000760.1:n.642+80G=
NM_000769.4:c.642+80G= MANE Select	NP_000760.1:n.642+80G=