Canonical Allele Identifier: CA1929298266

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94949113C= , CM000672.2:g.94949113C=	GRCh38
NC_000010.10:g.96708870C= , CM000672.1:g.96708870C=	GRCh37
NC_000010.9:g.96698860C=	NCBI36
NG_008385.1:g.15456C=
NG_008385.2:g.15956C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.648C= MANE Select	ENSP00000260682.6:p.Cys216=
ENST00000643112.1:c.648C=	ENSP00000496202.1:p.Cys216=
ENST00000260682.6:c.648C=	ENSP00000260682.6:p.Cys216=
ENST00000473496.1:n.419C=
NM_000771.3:c.648C=	NP_000762.2:p.Cys216=
NM_000771.4:c.648C= MANE Select	NP_000762.2:p.Cys216=