Canonical Allele Identifier: CA1929297878

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94948774G= , CM000672.2:g.94948774G=	GRCh38
NC_000010.10:g.96708531G= , CM000672.1:g.96708531G=	GRCh37
NC_000010.9:g.96698521G=	NCBI36
NG_008385.1:g.15117G=
NG_008385.2:g.15617G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.643-334G= MANE Select	ENSP00000260682.6:n.643-334G=
ENST00000643112.1:c.643-334G=	ENSP00000496202.1:n.643-334G=
ENST00000260682.6:c.643-334G=	ENSP00000260682.6:n.643-334G=
ENST00000473496.1:n.414-334G=
NM_000771.3:c.643-334G=	NP_000762.2:n.643-334G=
NM_000771.4:c.643-334G= MANE Select	NP_000762.2:n.643-334G=