Canonical Allele Identifier: CA1929292177

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941864A= , CM000672.2:g.94941864A=	GRCh38
NC_000010.10:g.96701621A= , CM000672.1:g.96701621A=	GRCh37
NC_000010.9:g.96691611A=	NCBI36
NG_008385.1:g.8207A=
NG_008385.2:g.8707A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.175A= MANE Select	ENSP00000260682.6:p.Lys59=
ENST00000643112.1:c.175A=	ENSP00000496202.1:p.Lys59=
ENST00000645207.1:n.328A=
ENST00000260682.6:c.175A=	ENSP00000260682.6:p.Lys59=
ENST00000461906.1:n.200A=
NM_000771.3:c.175A=	NP_000762.2:p.Lys59=
NM_000771.4:c.175A= MANE Select	NP_000762.2:p.Lys59=