Canonical Allele Identifier: CA1929341932

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981218A= , CM000672.2:g.94981218A=	GRCh38
NC_000010.10:g.96740975A= , CM000672.1:g.96740975A=	GRCh37
NC_000010.9:g.96730965A=	NCBI36
NG_008385.1:g.47561A=
NG_008385.2:g.48061A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.997A= MANE Select	ENSP00000260682.6:p.Arg333=
ENST00000643112.1:c.*6A=	ENSP00000496202.1:n.*6A=
ENST00000260682.6:c.997A=	ENSP00000260682.6:p.Arg333=
NM_000771.3:c.997A=	NP_000762.2:p.Arg333=
NM_000771.4:c.997A= MANE Select	NP_000762.2:p.Arg333=