Canonical Allele Identifier: CA2360465146
Gene: DNMT3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32805387G= , CM000682.2:g.32805387G= GRCh38
NC_000020.10:g.31393193G= , CM000682.1:g.31393193G= GRCh37
NC_000020.9:g.30856854G= NCBI36
NG_007290.1:g.48003G= , LRG_56:g.48003G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1232G= ENSP00000512497.1:n.*1232G=
ENST00000696232.1:c.2232-2375G= ENSP00000512498.1:n.2232-2375G=
ENST00000696233.1:c.*975-2375G= ENSP00000512499.1:n.*975-2375G=
ENST00000696238.1:c.*1024G= ENSP00000512502.1:n.*1024G=
ENST00000696239.1:c.2062G= ENSP00000512503.1:p.Glu688=
ENST00000696245.1:n.327-822G=
ENST00000201963.3:c.2257G= ENSP00000201963.3:p.Glu753=
ENST00000328111.6:c.2281G= MANE Select ENSP00000328547.2:p.Glu761=
ENST00000348286.6:c.2172-2375G= ENSP00000337764.2:n.2172-2375G=
ENST00000353855.6:c.2221G= ENSP00000313397.4:p.Glu741=
ENST00000443239.7:c.2046-2375G= ENSP00000403169.2:n.2046-2375G=
ENST00000456297.6:c.1944-2375G= ENSP00000412305.1:n.1944-2375G=
NM_001207055.1:c.2046-2375G= NP_001193984.1:n.2046-2375G=
NM_001207056.1:c.1944-2375G= NP_001193985.1:n.1944-2375G=
NM_006892.3:c.2281G= , LRG_56t1:c.2281G= NP_008823.1:p.Glu761=
NM_175848.1:c.2221G= NP_787044.1:p.Glu741=
NM_175849.1:c.2172-2375G= NP_787045.1:n.2172-2375G=
NM_175850.2:c.2257G= NP_787046.1:p.Glu753=
XM_011528653.1:c.2208-2375G= XP_011526955.1:n.2208-2375G=
XM_011528654.1:c.2082-2375G= XP_011526956.1:n.2082-2375G=
XR_936510.1:n.2248G=
XR_936511.1:n.2199-2375G=
XR_936512.1:n.2123G=
XM_011528653.2:c.2208-2375G= XP_011526955.1:n.2208-2375G=
XM_011528654.2:c.2082-2375G= XP_011526956.1:n.2082-2375G=
XR_936510.2:n.2259G=
XR_936511.2:n.2210-2375G=
XR_936512.2:n.2135G=
NM_001207055.2:c.2046-2375G= NP_001193984.1:n.2046-2375G=
NM_001207056.2:c.1944-2375G= NP_001193985.1:n.1944-2375G=
NM_006892.4:c.2281G= MANE Select NP_008823.1:p.Glu761=
NM_175848.2:c.2221G= NP_787044.1:p.Glu741=
NM_175849.2:c.2172-2375G= NP_787045.1:n.2172-2375G=
NM_175850.3:c.2257G= NP_787046.1:p.Glu753=