Canonical Allele Identifier: CA1929292199

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941907C= , CM000672.2:g.94941907C=	GRCh38
NC_000010.10:g.96701664C= , CM000672.1:g.96701664C=	GRCh37
NC_000010.9:g.96691654C=	NCBI36
NG_008385.1:g.8250C=
NG_008385.2:g.8750C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.218C= MANE Select	ENSP00000260682.6:p.Pro73=
ENST00000643112.1:c.218C=	ENSP00000496202.1:p.Pro73=
ENST00000645207.1:n.371C=
ENST00000260682.6:c.218C=	ENSP00000260682.6:p.Pro73=
ENST00000461906.1:n.243C=
NM_000771.3:c.218C=	NP_000762.2:p.Pro73=
NM_000771.4:c.218C= MANE Select	NP_000762.2:p.Pro73=