Canonical Allele Identifier: CA1929292370

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942166C= , CM000672.2:g.94942166C=	GRCh38
NC_000010.10:g.96701923C= , CM000672.1:g.96701923C=	GRCh37
NC_000010.9:g.96691913C=	NCBI36
NG_008385.1:g.8509C=
NG_008385.2:g.9009C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.332-26C= MANE Select	ENSP00000260682.6:n.332-26C=
ENST00000643112.1:c.332-26C=	ENSP00000496202.1:n.332-26C=
ENST00000645207.1:n.485-26C=
ENST00000260682.6:c.332-26C=	ENSP00000260682.6:n.332-26C=
ENST00000461906.1:n.357-26C=
ENST00000473496.1:n.103-26C=
NM_000771.3:c.332-26C=	NP_000762.2:n.332-26C=
NM_000771.4:c.332-26C= MANE Select	NP_000762.2:n.332-26C=