Canonical Allele Identifier: CA2360465139

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805369G= , CM000682.2:g.32805369G=	GRCh38
NC_000020.10:g.31393175G= , CM000682.1:g.31393175G=	GRCh37
NC_000020.9:g.30856836G=	NCBI36
NG_007290.1:g.47985G= , LRG_56:g.47985G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1214G=	ENSP00000512497.1:n.*1214G=
ENST00000696232.1:c.2232-2393G=	ENSP00000512498.1:n.2232-2393G=
ENST00000696233.1:c.*975-2393G=	ENSP00000512499.1:n.*975-2393G=
ENST00000696238.1:c.*1006G=	ENSP00000512502.1:n.*1006G=
ENST00000696239.1:c.2044G=	ENSP00000512503.1:p.Glu682=
ENST00000696245.1:n.327-840G=
ENST00000201963.3:c.2239G=	ENSP00000201963.3:p.Glu747=
ENST00000328111.6:c.2263G= MANE Select	ENSP00000328547.2:p.Glu755=
ENST00000348286.6:c.2172-2393G=	ENSP00000337764.2:n.2172-2393G=
ENST00000353855.6:c.2203G=	ENSP00000313397.4:p.Glu735=
ENST00000443239.7:c.2046-2393G=	ENSP00000403169.2:n.2046-2393G=
ENST00000456297.6:c.1944-2393G=	ENSP00000412305.1:n.1944-2393G=
NM_001207055.1:c.2046-2393G=	NP_001193984.1:n.2046-2393G=
NM_001207056.1:c.1944-2393G=	NP_001193985.1:n.1944-2393G=
NM_006892.3:c.2263G= , LRG_56t1:c.2263G=	NP_008823.1:p.Glu755=
NM_175848.1:c.2203G=	NP_787044.1:p.Glu735=
NM_175849.1:c.2172-2393G=	NP_787045.1:n.2172-2393G=
NM_175850.2:c.2239G=	NP_787046.1:p.Glu747=
XM_011528653.1:c.2208-2393G=	XP_011526955.1:n.2208-2393G=
XM_011528654.1:c.2082-2393G=	XP_011526956.1:n.2082-2393G=
XR_936510.1:n.2230G=
XR_936511.1:n.2199-2393G=
XR_936512.1:n.2105G=
XM_011528653.2:c.2208-2393G=	XP_011526955.1:n.2208-2393G=
XM_011528654.2:c.2082-2393G=	XP_011526956.1:n.2082-2393G=
XR_936510.2:n.2241G=
XR_936511.2:n.2210-2393G=
XR_936512.2:n.2117G=
NM_001207055.2:c.2046-2393G=	NP_001193984.1:n.2046-2393G=
NM_001207056.2:c.1944-2393G=	NP_001193985.1:n.1944-2393G=
NM_006892.4:c.2263G= MANE Select	NP_008823.1:p.Glu755=
NM_175848.2:c.2203G=	NP_787044.1:p.Glu735=
NM_175849.2:c.2172-2393G=	NP_787045.1:n.2172-2393G=
NM_175850.3:c.2239G=	NP_787046.1:p.Glu747=