Canonical Allele Identifier: CA1929222875

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94782174T= , CM000672.2:g.94782174T=	GRCh38
NC_000010.10:g.96541931T= , CM000672.1:g.96541931T=	GRCh37
NC_000010.9:g.96531921T=	NCBI36
NG_008384.2:g.24469T=
NG_008384.3:g.24494T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.819+177T= MANE Select	ENSP00000360372.3:n.819+177T=
ENST00000645461.1:n.1872+177T=
ENST00000371321.7:c.819+177T=	ENSP00000360372.3:n.819+177T=
ENST00000464755.1:c.1582+177T=	ENSP00000483243.1:n.1582+177T=
NM_000769.2:c.819+177T=	NP_000760.1:n.819+177T=
NM_000769.4:c.819+177T= MANE Select	NP_000760.1:n.819+177T=