Canonical Allele Identifier: CA1929292105

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941746T= , CM000672.2:g.94941746T=	GRCh38
NC_000010.10:g.96701503T= , CM000672.1:g.96701503T=	GRCh37
NC_000010.9:g.96691493T=	NCBI36
NG_008385.1:g.8089T=
NG_008385.2:g.8589T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-112T= MANE Select	ENSP00000260682.6:n.169-112T=
ENST00000643112.1:c.169-112T=	ENSP00000496202.1:n.169-112T=
ENST00000645207.1:n.210T=
ENST00000260682.6:c.169-112T=	ENSP00000260682.6:n.169-112T=
ENST00000461906.1:n.194-112T=
NM_000771.3:c.169-112T=	NP_000762.2:n.169-112T=
NM_000771.4:c.169-112T= MANE Select	NP_000762.2:n.169-112T=