Canonical Allele Identifier: CA1929342171

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981312C= , CM000672.2:g.94981312C=	GRCh38
NC_000010.10:g.96741069C= , CM000672.1:g.96741069C=	GRCh37
NC_000010.9:g.96731059C=	NCBI36
NG_008385.1:g.47655C=
NG_008385.2:g.48155C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1091C= MANE Select	ENSP00000260682.6:p.Thr364=
ENST00000643112.1:c.*100C=	ENSP00000496202.1:n.*100C=
ENST00000260682.6:c.1091C=	ENSP00000260682.6:p.Thr364=
NM_000771.3:c.1091C=	NP_000762.2:p.Thr364=
NM_000771.4:c.1091C= MANE Select	NP_000762.2:p.Thr364=