Canonical Allele Identifier: CA1929349639

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94988906T= , CM000672.2:g.94988906T=	GRCh38
NC_000010.10:g.96748663T= , CM000672.1:g.96748663T=	GRCh37
NC_000010.9:g.96738653T=	NCBI36
NG_008385.1:g.55249T=
NG_008385.2:g.55749T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1351T= MANE Select	ENSP00000260682.6:p.Ser451=
ENST00000643112.1:c.*360T=	ENSP00000496202.1:n.*360T=
ENST00000260682.6:c.1351T=	ENSP00000260682.6:p.Ser451=
NM_000771.3:c.1351T=	NP_000762.2:p.Ser451=
NM_000771.4:c.1351T= MANE Select	NP_000762.2:p.Ser451=