Canonical Allele Identifier: CA1929342174

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981315G= , CM000672.2:g.94981315G=	GRCh38
NC_000010.10:g.96741072G= , CM000672.1:g.96741072G=	GRCh37
NC_000010.9:g.96731062G=	NCBI36
NG_008385.1:g.47658G=
NG_008385.2:g.48158G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1094G= MANE Select	ENSP00000260682.6:p.Ser365=
ENST00000643112.1:c.*103G=	ENSP00000496202.1:n.*103G=
ENST00000260682.6:c.1094G=	ENSP00000260682.6:p.Ser365=
NM_000771.3:c.1094G=	NP_000762.2:p.Ser365=
NM_000771.4:c.1094G= MANE Select	NP_000762.2:p.Ser365=