Canonical Allele Identifier: CA408586984
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32787430T>G , CM000682.2:g.32787430T>G GRCh38
NC_000020.10:g.31375236T>G , CM000682.1:g.31375236T>G GRCh37
NC_000020.9:g.30838897T>G NCBI36
NG_007290.1:g.30046T>G , LRG_56:g.30046T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.633T>G ENSP00000512497.1:p.Asp211Glu
ENST00000696232.1:c.633T>G ENSP00000512498.1:p.Asp211Glu
ENST00000696233.1:c.633T>G ENSP00000512499.1:p.Asp211Glu
ENST00000696234.1:n.617T>G
ENST00000696235.1:c.507T>G ENSP00000512500.1:p.Asp169Glu
ENST00000696236.1:c.507T>G ENSP00000512501.1:p.Asp169Glu
ENST00000696237.1:n.739T>G
ENST00000696238.1:c.633T>G ENSP00000512502.1:p.Asp211Glu
ENST00000696239.1:c.633T>G ENSP00000512503.1:p.Asp211Glu
ENST00000201963.3:c.669T>G ENSP00000201963.3:p.Asp223Glu
ENST00000328111.6:c.633T>G MANE Select ENSP00000328547.2:p.Asp211Glu
ENST00000348286.6:c.633T>G ENSP00000337764.2:p.Asp211Glu
ENST00000353855.6:c.633T>G ENSP00000313397.4:p.Asp211Glu
ENST00000443239.7:c.507T>G ENSP00000403169.2:p.Asp169Glu
ENST00000456297.6:c.405T>G ENSP00000412305.1:p.Asp135Glu
NM_001207055.1:c.507T>G NP_001193984.1:p.Asp169Glu
NM_001207056.1:c.405T>G NP_001193985.1:p.Asp135Glu
NM_006892.3:c.633T>G , LRG_56t1:c.633T>G NP_008823.1:p.Asp211Glu
NM_175848.1:c.633T>G NP_787044.1:p.Asp211Glu
NM_175849.1:c.633T>G NP_787045.1:p.Asp211Glu
NM_175850.2:c.669T>G NP_787046.1:p.Asp223Glu
XM_011528653.1:c.669T>G XP_011526955.1:p.Asp223Glu
XM_011528654.1:c.543T>G XP_011526956.1:p.Asp181Glu
XR_936510.1:n.805T>G
XR_936511.1:n.805T>G
XR_936512.1:n.680T>G
XM_011528653.2:c.669T>G XP_011526955.1:p.Asp223Glu
XM_011528654.2:c.543T>G XP_011526956.1:p.Asp181Glu
XR_936510.2:n.816T>G
XR_936511.2:n.816T>G
XR_936512.2:n.692T>G
NM_001207055.2:c.507T>G NP_001193984.1:p.Asp169Glu
NM_001207056.2:c.405T>G NP_001193985.1:p.Asp135Glu
NM_006892.4:c.633T>G MANE Select NP_008823.1:p.Asp211Glu
NM_175848.2:c.633T>G NP_787044.1:p.Asp211Glu
NM_175849.2:c.633T>G NP_787045.1:p.Asp211Glu
NM_175850.3:c.669T>G NP_787046.1:p.Asp223Glu