Canonical Allele Identifier: CA1929334786

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974513C= , CM000672.2:g.94974513C=	GRCh38
NC_000010.10:g.96734270C= , CM000672.1:g.96734270C=	GRCh37
NC_000010.9:g.96724260C=	NCBI36
NG_008385.1:g.40856C=
NG_008385.2:g.41356C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.961+2268C= MANE Select	ENSP00000260682.6:n.961+2268C=
ENST00000643112.1:c.820-6670C=	ENSP00000496202.1:n.820-6670C=
ENST00000260682.6:c.961+2268C=	ENSP00000260682.6:n.961+2268C=
NM_000771.3:c.961+2268C=	NP_000762.2:n.961+2268C=
NM_000771.4:c.961+2268C= MANE Select	NP_000762.2:n.961+2268C=