Canonical Allele Identifier: CA1929278469

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850285A= , CM000672.2:g.94850285A=	GRCh38
NC_000010.10:g.96610042A= , CM000672.1:g.96610042A=	GRCh37
NC_000010.9:g.96600032A=	NCBI36
NG_008384.2:g.92580A=
NG_008384.3:g.92605A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1291+227A= MANE Select	ENSP00000360372.3:n.1291+227A=
ENST00000645461.1:n.2202+227A=
ENST00000371321.7:c.1291+227A=	ENSP00000360372.3:n.1291+227A=
ENST00000464755.1:c.2054+227A=	ENSP00000483243.1:n.2054+227A=
NM_000769.2:c.1291+227A=	NP_000760.1:n.1291+227A=
NM_000769.4:c.1291+227A= MANE Select	NP_000760.1:n.1291+227A=