Canonical Allele Identifier: CA1929349571

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94988884G= , CM000672.2:g.94988884G=	GRCh38
NC_000010.10:g.96748641G= , CM000672.1:g.96748641G=	GRCh37
NC_000010.9:g.96738631G=	NCBI36
NG_008385.1:g.55227G=
NG_008385.2:g.55727G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1329G= MANE Select	ENSP00000260682.6:p.Met443=
ENST00000643112.1:c.*338G=	ENSP00000496202.1:n.*338G=
ENST00000260682.6:c.1329G=	ENSP00000260682.6:p.Met443=
NM_000771.3:c.1329G=	NP_000762.2:p.Met443=
NM_000771.4:c.1329G= MANE Select	NP_000762.2:p.Met443=