Canonical Allele Identifier: CA1929292256

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942006C= , CM000672.2:g.94942006C=	GRCh38
NC_000010.10:g.96701763C= , CM000672.1:g.96701763C=	GRCh37
NC_000010.9:g.96691753C=	NCBI36
NG_008385.1:g.8349C=
NG_008385.2:g.8849C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.317C= MANE Select	ENSP00000260682.6:p.Ala106=
ENST00000643112.1:c.317C=	ENSP00000496202.1:p.Ala106=
ENST00000645207.1:n.470C=
ENST00000260682.6:c.317C=	ENSP00000260682.6:p.Ala106=
ENST00000461906.1:n.342C=
ENST00000473496.1:n.88C=
NM_000771.3:c.317C=	NP_000762.2:p.Ala106=
NM_000771.4:c.317C= MANE Select	NP_000762.2:p.Ala106=