Canonical Allele Identifier: CA1929297886

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94948776A= , CM000672.2:g.94948776A=	GRCh38
NC_000010.10:g.96708533A= , CM000672.1:g.96708533A=	GRCh37
NC_000010.9:g.96698523A=	NCBI36
NG_008385.1:g.15119A=
NG_008385.2:g.15619A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.643-332A= MANE Select	ENSP00000260682.6:n.643-332A=
ENST00000643112.1:c.643-332A=	ENSP00000496202.1:n.643-332A=
ENST00000260682.6:c.643-332A=	ENSP00000260682.6:n.643-332A=
ENST00000473496.1:n.414-332A=
NM_000771.3:c.643-332A=	NP_000762.2:n.643-332A=
NM_000771.4:c.643-332A= MANE Select	NP_000762.2:n.643-332A=