Canonical Allele Identifier: CA408588547
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32800287A>G , CM000682.2:g.32800287A>G GRCh38
NC_000020.10:g.31388093A>G , CM000682.1:g.31388093A>G GRCh37
NC_000020.9:g.30851754A>G NCBI36
NG_007290.1:g.42903A>G , LRG_56:g.42903A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*845A>G ENSP00000512497.1:n.*845A>G
ENST00000696232.1:c.1894A>G ENSP00000512498.1:p.Thr632Ala
ENST00000696233.1:c.*637A>G ENSP00000512499.1:n.*637A>G
ENST00000696235.1:c.*542A>G ENSP00000512500.1:n.*542A>G
ENST00000696238.1:c.*637A>G ENSP00000512502.1:n.*637A>G
ENST00000696239.1:c.1675A>G ENSP00000512503.1:p.Thr559Ala
ENST00000201963.3:c.1870A>G ENSP00000201963.3:p.Thr624Ala
ENST00000328111.6:c.1894A>G MANE Select ENSP00000328547.2:p.Thr632Ala
ENST00000348286.6:c.1834A>G ENSP00000337764.2:p.Thr612Ala
ENST00000353855.6:c.1834A>G ENSP00000313397.4:p.Thr612Ala
ENST00000443239.7:c.1708A>G ENSP00000403169.2:p.Thr570Ala
ENST00000456297.6:c.1606A>G ENSP00000412305.1:p.Thr536Ala
NM_001207055.1:c.1708A>G NP_001193984.1:p.Thr570Ala
NM_001207056.1:c.1606A>G NP_001193985.1:p.Thr536Ala
NM_006892.3:c.1894A>G , LRG_56t1:c.1894A>G NP_008823.1:p.Thr632Ala
NM_175848.1:c.1834A>G NP_787044.1:p.Thr612Ala
NM_175849.1:c.1834A>G NP_787045.1:p.Thr612Ala
NM_175850.2:c.1870A>G NP_787046.1:p.Thr624Ala
XM_011528653.1:c.1870A>G XP_011526955.1:p.Thr624Ala
XM_011528654.1:c.1744A>G XP_011526956.1:p.Thr582Ala
XR_936510.1:n.1861A>G
XR_936511.1:n.1861A>G
XR_936512.1:n.1736A>G
XM_011528653.2:c.1870A>G XP_011526955.1:p.Thr624Ala
XM_011528654.2:c.1744A>G XP_011526956.1:p.Thr582Ala
XR_936510.2:n.1872A>G
XR_936511.2:n.1872A>G
XR_936512.2:n.1748A>G
NM_001207055.2:c.1708A>G NP_001193984.1:p.Thr570Ala
NM_001207056.2:c.1606A>G NP_001193985.1:p.Thr536Ala
NM_006892.4:c.1894A>G MANE Select NP_008823.1:p.Thr632Ala
NM_175848.2:c.1834A>G NP_787044.1:p.Thr612Ala
NM_175849.2:c.1834A>G NP_787045.1:p.Thr612Ala
NM_175850.3:c.1870A>G NP_787046.1:p.Thr624Ala