Canonical Allele Identifier: CA1929297937

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94948836T= , CM000672.2:g.94948836T=	GRCh38
NC_000010.10:g.96708593T= , CM000672.1:g.96708593T=	GRCh37
NC_000010.9:g.96698583T=	NCBI36
NG_008385.1:g.15179T=
NG_008385.2:g.15679T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.643-272T= MANE Select	ENSP00000260682.6:n.643-272T=
ENST00000643112.1:c.643-272T=	ENSP00000496202.1:n.643-272T=
ENST00000260682.6:c.643-272T=	ENSP00000260682.6:n.643-272T=
ENST00000473496.1:n.414-272T=
NM_000771.3:c.643-272T=	NP_000762.2:n.643-272T=
NM_000771.4:c.643-272T= MANE Select	NP_000762.2:n.643-272T=