Canonical Allele Identifier: CA1929221713

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780783C= , CM000672.2:g.94780783C=	GRCh38
NC_000010.10:g.96540540C= , CM000672.1:g.96540540C=	GRCh37
NC_000010.9:g.96530530C=	NCBI36
NG_008384.2:g.23078C=
NG_008384.3:g.23103C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.642+124C= MANE Select	ENSP00000360372.3:n.642+124C=
ENST00000645461.1:n.1695+124C=
ENST00000371321.7:c.642+124C=	ENSP00000360372.3:n.642+124C=
ENST00000464755.1:c.1405+124C=	ENSP00000483243.1:n.1405+124C=
NM_000769.2:c.642+124C=	NP_000760.1:n.642+124C=
NM_000769.4:c.642+124C= MANE Select	NP_000760.1:n.642+124C=