Canonical Allele Identifier: CA408588425
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32800228C>T , CM000682.2:g.32800228C>T GRCh38
NC_000020.10:g.31388034C>T , CM000682.1:g.31388034C>T GRCh37
NC_000020.9:g.30851695C>T NCBI36
NG_007290.1:g.42844C>T , LRG_56:g.42844C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*786C>T ENSP00000512497.1:n.*786C>T
ENST00000696232.1:c.1835C>T ENSP00000512498.1:p.Ala612Val
ENST00000696233.1:c.*578C>T ENSP00000512499.1:n.*578C>T
ENST00000696235.1:c.*483C>T ENSP00000512500.1:n.*483C>T
ENST00000696238.1:c.*578C>T ENSP00000512502.1:n.*578C>T
ENST00000696239.1:c.1616C>T ENSP00000512503.1:p.Ala539Val
ENST00000201963.3:c.1811C>T ENSP00000201963.3:p.Ala604Val
ENST00000328111.6:c.1835C>T MANE Select ENSP00000328547.2:p.Ala612Val
ENST00000348286.6:c.1775C>T ENSP00000337764.2:p.Ala592Val
ENST00000353855.6:c.1775C>T ENSP00000313397.4:p.Ala592Val
ENST00000443239.7:c.1649C>T ENSP00000403169.2:p.Ala550Val
ENST00000456297.6:c.1547C>T ENSP00000412305.1:p.Ala516Val
NM_001207055.1:c.1649C>T NP_001193984.1:p.Ala550Val
NM_001207056.1:c.1547C>T NP_001193985.1:p.Ala516Val
NM_006892.3:c.1835C>T , LRG_56t1:c.1835C>T NP_008823.1:p.Ala612Val
NM_175848.1:c.1775C>T NP_787044.1:p.Ala592Val
NM_175849.1:c.1775C>T NP_787045.1:p.Ala592Val
NM_175850.2:c.1811C>T NP_787046.1:p.Ala604Val
XM_011528653.1:c.1811C>T XP_011526955.1:p.Ala604Val
XM_011528654.1:c.1685C>T XP_011526956.1:p.Ala562Val
XR_936510.1:n.1802C>T
XR_936511.1:n.1802C>T
XR_936512.1:n.1677C>T
XM_011528653.2:c.1811C>T XP_011526955.1:p.Ala604Val
XM_011528654.2:c.1685C>T XP_011526956.1:p.Ala562Val
XR_936510.2:n.1813C>T
XR_936511.2:n.1813C>T
XR_936512.2:n.1689C>T
NM_001207055.2:c.1649C>T NP_001193984.1:p.Ala550Val
NM_001207056.2:c.1547C>T NP_001193985.1:p.Ala516Val
NM_006892.4:c.1835C>T MANE Select NP_008823.1:p.Ala612Val
NM_175848.2:c.1775C>T NP_787044.1:p.Ala592Val
NM_175849.2:c.1775C>T NP_787045.1:p.Ala592Val
NM_175850.3:c.1811C>T NP_787046.1:p.Ala604Val