Canonical Allele Identifier: CA1929349523

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94988869A= , CM000672.2:g.94988869A=	GRCh38
NC_000010.10:g.96748626A= , CM000672.1:g.96748626A=	GRCh37
NC_000010.9:g.96738616A=	NCBI36
NG_008385.1:g.55212A=
NG_008385.2:g.55712A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1314A= MANE Select	ENSP00000260682.6:p.Glu438=
ENST00000643112.1:c.*323A=	ENSP00000496202.1:n.*323A=
ENST00000260682.6:c.1314A=	ENSP00000260682.6:p.Glu438=
NM_000771.3:c.1314A=	NP_000762.2:p.Glu438=
NM_000771.4:c.1314A= MANE Select	NP_000762.2:p.Glu438=