Canonical Allele Identifier: CA1929218612

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775156T= , CM000672.2:g.94775156T=	GRCh38
NC_000010.10:g.96534913T= , CM000672.1:g.96534913T=	GRCh37
NC_000010.9:g.96524903T=	NCBI36
NG_008384.2:g.17451T=
NG_008384.3:g.17476T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.267T= MANE Select	ENSP00000360372.3:p.Asp89=
ENST00000645461.1:n.1320T=
ENST00000371321.7:c.267T=	ENSP00000360372.3:p.Asp89=
ENST00000464755.1:c.1030T=	ENSP00000483243.1:n.1030T=
ENST00000480405.2:c.267T=	ENSP00000483847.1:p.Asp89=
NM_000769.2:c.267T=	NP_000760.1:p.Asp89=
NM_000769.4:c.267T= MANE Select	NP_000760.1:p.Asp89=