Canonical Allele Identifier: CA1929297924

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94948813A= , CM000672.2:g.94948813A=	GRCh38
NC_000010.10:g.96708570A= , CM000672.1:g.96708570A=	GRCh37
NC_000010.9:g.96698560A=	NCBI36
NG_008385.1:g.15156A=
NG_008385.2:g.15656A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.643-295A= MANE Select	ENSP00000260682.6:n.643-295A=
ENST00000643112.1:c.643-295A=	ENSP00000496202.1:n.643-295A=
ENST00000260682.6:c.643-295A=	ENSP00000260682.6:n.643-295A=
ENST00000473496.1:n.414-295A=
NM_000771.3:c.643-295A=	NP_000762.2:n.643-295A=
NM_000771.4:c.643-295A= MANE Select	NP_000762.2:n.643-295A=