Canonical Allele Identifier: CA1929298286

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94949131C= , CM000672.2:g.94949131C=	GRCh38
NC_000010.10:g.96708888C= , CM000672.1:g.96708888C=	GRCh37
NC_000010.9:g.96698878C=	NCBI36
NG_008385.1:g.15474C=
NG_008385.2:g.15974C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.666C= MANE Select	ENSP00000260682.6:p.Ile222=
ENST00000643112.1:c.666C=	ENSP00000496202.1:p.Ile222=
ENST00000260682.6:c.666C=	ENSP00000260682.6:p.Ile222=
ENST00000473496.1:n.437C=
NM_000771.3:c.666C=	NP_000762.2:p.Ile222=
NM_000771.4:c.666C= MANE Select	NP_000762.2:p.Ile222=