Canonical Allele Identifier: CA1929341921

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981210T= , CM000672.2:g.94981210T=	GRCh38
NC_000010.10:g.96740967T= , CM000672.1:g.96740967T=	GRCh37
NC_000010.9:g.96730957T=	NCBI36
NG_008385.1:g.47553T=
NG_008385.2:g.48053T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.989T= MANE Select	ENSP00000260682.6:p.Val330=
ENST00000643112.1:c.847T=	ENSP00000496202.1:p.Ter283=
ENST00000260682.6:c.989T=	ENSP00000260682.6:p.Val330=
NM_000771.3:c.989T=	NP_000762.2:p.Val330=
NM_000771.4:c.989T= MANE Select	NP_000762.2:p.Val330=