Canonical Allele Identifier: CA1929279998

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852987C= , CM000672.2:g.94852987C=	GRCh38
NC_000010.10:g.96612744C= , CM000672.1:g.96612744C=	GRCh37
NC_000010.9:g.96602734C=	NCBI36
NG_008384.2:g.95282C=
NG_008384.3:g.95307C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.*73C= MANE Select	ENSP00000360372.3:n.*73C=
ENST00000645461.1:n.2457C=
ENST00000371321.7:c.*73C=	ENSP00000360372.3:n.*73C=
ENST00000464755.1:c.2309C=	ENSP00000483243.1:n.2309C=
NM_000769.2:c.*73C=	NP_000760.1:n.*73C=
NM_000769.4:c.*73C= MANE Select	NP_000760.1:n.*73C=