Canonical Allele Identifier: CA1929218597

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775123T= , CM000672.2:g.94775123T=	GRCh38
NC_000010.10:g.96534880T= , CM000672.1:g.96534880T=	GRCh37
NC_000010.9:g.96524870T=	NCBI36
NG_008384.2:g.17418T=
NG_008384.3:g.17443T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.234T= MANE Select	ENSP00000360372.3:p.His78=
ENST00000645461.1:n.1287T=
ENST00000371321.7:c.234T=	ENSP00000360372.3:p.His78=
ENST00000464755.1:c.997T=	ENSP00000483243.1:p.Trp333=
ENST00000480405.2:c.234T=	ENSP00000483847.1:p.His78=
NM_000769.2:c.234T=	NP_000760.1:p.His78=
NM_000769.4:c.234T= MANE Select	NP_000760.1:p.His78=