Canonical Allele Identifier: CA1929341890

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981192A= , CM000672.2:g.94981192A=	GRCh38
NC_000010.10:g.96740949A= , CM000672.1:g.96740949A=	GRCh37
NC_000010.9:g.96730939A=	NCBI36
NG_008385.1:g.47535A=
NG_008385.2:g.48035A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.971A= MANE Select	ENSP00000260682.6:p.Gln324=
ENST00000643112.1:c.829A=	ENSP00000496202.1:p.Arg277=
ENST00000260682.6:c.971A=	ENSP00000260682.6:p.Gln324=
NM_000771.3:c.971A=	NP_000762.2:p.Gln324=
NM_000771.4:c.971A= MANE Select	NP_000762.2:p.Gln324=