Canonical Allele Identifier: CA408588349
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32800203T>G , CM000682.2:g.32800203T>G GRCh38
NC_000020.10:g.31388009T>G , CM000682.1:g.31388009T>G GRCh37
NC_000020.9:g.30851670T>G NCBI36
NG_007290.1:g.42819T>G , LRG_56:g.42819T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*761T>G ENSP00000512497.1:n.*761T>G
ENST00000696232.1:c.1810T>G ENSP00000512498.1:p.Ser604Ala
ENST00000696233.1:c.*553T>G ENSP00000512499.1:n.*553T>G
ENST00000696235.1:c.*458T>G ENSP00000512500.1:n.*458T>G
ENST00000696238.1:c.*553T>G ENSP00000512502.1:n.*553T>G
ENST00000696239.1:c.1591T>G ENSP00000512503.1:p.Ser531Ala
ENST00000201963.3:c.1786T>G ENSP00000201963.3:p.Ser596Ala
ENST00000328111.6:c.1810T>G MANE Select ENSP00000328547.2:p.Ser604Ala
ENST00000348286.6:c.1750T>G ENSP00000337764.2:p.Ser584Ala
ENST00000353855.6:c.1750T>G ENSP00000313397.4:p.Ser584Ala
ENST00000443239.7:c.1624T>G ENSP00000403169.2:p.Ser542Ala
ENST00000456297.6:c.1522T>G ENSP00000412305.1:p.Ser508Ala
NM_001207055.1:c.1624T>G NP_001193984.1:p.Ser542Ala
NM_001207056.1:c.1522T>G NP_001193985.1:p.Ser508Ala
NM_006892.3:c.1810T>G , LRG_56t1:c.1810T>G NP_008823.1:p.Ser604Ala
NM_175848.1:c.1750T>G NP_787044.1:p.Ser584Ala
NM_175849.1:c.1750T>G NP_787045.1:p.Ser584Ala
NM_175850.2:c.1786T>G NP_787046.1:p.Ser596Ala
XM_011528653.1:c.1786T>G XP_011526955.1:p.Ser596Ala
XM_011528654.1:c.1660T>G XP_011526956.1:p.Ser554Ala
XR_936510.1:n.1777T>G
XR_936511.1:n.1777T>G
XR_936512.1:n.1652T>G
XM_011528653.2:c.1786T>G XP_011526955.1:p.Ser596Ala
XM_011528654.2:c.1660T>G XP_011526956.1:p.Ser554Ala
XR_936510.2:n.1788T>G
XR_936511.2:n.1788T>G
XR_936512.2:n.1664T>G
NM_001207055.2:c.1624T>G NP_001193984.1:p.Ser542Ala
NM_001207056.2:c.1522T>G NP_001193985.1:p.Ser508Ala
NM_006892.4:c.1810T>G MANE Select NP_008823.1:p.Ser604Ala
NM_175848.2:c.1750T>G NP_787044.1:p.Ser584Ala
NM_175849.2:c.1750T>G NP_787045.1:p.Ser584Ala
NM_175850.3:c.1786T>G NP_787046.1:p.Ser596Ala