Canonical Allele Identifier: CA2360456948

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787242C= , CM000682.2:g.32787242C=	GRCh38
NC_000020.10:g.31375048C= , CM000682.1:g.31375048C=	GRCh37
NC_000020.9:g.30838709C=	NCBI36
NG_007290.1:g.29858C= , LRG_56:g.29858C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.445C=	ENSP00000512497.1:p.Arg149=
ENST00000696232.1:c.445C=	ENSP00000512498.1:p.Arg149=
ENST00000696233.1:c.445C=	ENSP00000512499.1:p.Arg149=
ENST00000696234.1:n.429C=
ENST00000696235.1:c.319C=	ENSP00000512500.1:p.Arg107=
ENST00000696236.1:c.319C=	ENSP00000512501.1:p.Arg107=
ENST00000696237.1:n.551C=
ENST00000696238.1:c.445C=	ENSP00000512502.1:p.Arg149=
ENST00000696239.1:c.445C=	ENSP00000512503.1:p.Arg149=
ENST00000201963.3:c.481C=	ENSP00000201963.3:p.Arg161=
ENST00000328111.6:c.445C= MANE Select	ENSP00000328547.2:p.Arg149=
ENST00000348286.6:c.445C=	ENSP00000337764.2:p.Arg149=
ENST00000353855.6:c.445C=	ENSP00000313397.4:p.Arg149=
ENST00000443239.7:c.319C=	ENSP00000403169.2:p.Arg107=
ENST00000456297.6:c.217C=	ENSP00000412305.1:p.Arg73=
NM_001207055.1:c.319C=	NP_001193984.1:p.Arg107=
NM_001207056.1:c.217C=	NP_001193985.1:p.Arg73=
NM_006892.3:c.445C= , LRG_56t1:c.445C=	NP_008823.1:p.Arg149=
NM_175848.1:c.445C=	NP_787044.1:p.Arg149=
NM_175849.1:c.445C=	NP_787045.1:p.Arg149=
NM_175850.2:c.481C=	NP_787046.1:p.Arg161=
XM_011528653.1:c.481C=	XP_011526955.1:p.Arg161=
XM_011528654.1:c.355C=	XP_011526956.1:p.Arg119=
XR_936510.1:n.617C=
XR_936511.1:n.617C=
XR_936512.1:n.492C=
XM_011528653.2:c.481C=	XP_011526955.1:p.Arg161=
XM_011528654.2:c.355C=	XP_011526956.1:p.Arg119=
XR_936510.2:n.628C=
XR_936511.2:n.628C=
XR_936512.2:n.504C=
NM_001207055.2:c.319C=	NP_001193984.1:p.Arg107=
NM_001207056.2:c.217C=	NP_001193985.1:p.Arg73=
NM_006892.4:c.445C= MANE Select	NP_008823.1:p.Arg149=
NM_175848.2:c.445C=	NP_787044.1:p.Arg149=
NM_175849.2:c.445C=	NP_787045.1:p.Arg149=
NM_175850.3:c.481C=	NP_787046.1:p.Arg161=