Canonical Allele Identifier: CA1929292182

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941874G= , CM000672.2:g.94941874G=	GRCh38
NC_000010.10:g.96701631G= , CM000672.1:g.96701631G=	GRCh37
NC_000010.9:g.96691621G=	NCBI36
NG_008385.1:g.8217G=
NG_008385.2:g.8717G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.185G= MANE Select	ENSP00000260682.6:p.Gly62=
ENST00000643112.1:c.185G=	ENSP00000496202.1:p.Gly62=
ENST00000645207.1:n.338G=
ENST00000260682.6:c.185G=	ENSP00000260682.6:p.Gly62=
ENST00000461906.1:n.210G=
NM_000771.3:c.185G=	NP_000762.2:p.Gly62=
NM_000771.4:c.185G= MANE Select	NP_000762.2:p.Gly62=