Canonical Allele Identifier: CA1929292193

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941899C= , CM000672.2:g.94941899C=	GRCh38
NC_000010.10:g.96701656C= , CM000672.1:g.96701656C=	GRCh37
NC_000010.9:g.96691646C=	NCBI36
NG_008385.1:g.8242C=
NG_008385.2:g.8742C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.210C= MANE Select	ENSP00000260682.6:p.Gly70=
ENST00000643112.1:c.210C=	ENSP00000496202.1:p.Gly70=
ENST00000645207.1:n.363C=
ENST00000260682.6:c.210C=	ENSP00000260682.6:p.Gly70=
ENST00000461906.1:n.235C=
NM_000771.3:c.210C=	NP_000762.2:p.Gly70=
NM_000771.4:c.210C= MANE Select	NP_000762.2:p.Gly70=