Canonical Allele Identifier: CA408586901
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32787409G>T , CM000682.2:g.32787409G>T GRCh38
NC_000020.10:g.31375215G>T , CM000682.1:g.31375215G>T GRCh37
NC_000020.9:g.30838876G>T NCBI36
NG_007290.1:g.30025G>T , LRG_56:g.30025G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.612G>T ENSP00000512497.1:p.Gln204His
ENST00000696232.1:c.612G>T ENSP00000512498.1:p.Gln204His
ENST00000696233.1:c.612G>T ENSP00000512499.1:p.Gln204His
ENST00000696234.1:n.596G>T
ENST00000696235.1:c.486G>T ENSP00000512500.1:p.Gln162His
ENST00000696236.1:c.486G>T ENSP00000512501.1:p.Gln162His
ENST00000696237.1:n.718G>T
ENST00000696238.1:c.612G>T ENSP00000512502.1:p.Gln204His
ENST00000696239.1:c.612G>T ENSP00000512503.1:p.Gln204His
ENST00000201963.3:c.648G>T ENSP00000201963.3:p.Gln216His
ENST00000328111.6:c.612G>T MANE Select ENSP00000328547.2:p.Gln204His
ENST00000348286.6:c.612G>T ENSP00000337764.2:p.Gln204His
ENST00000353855.6:c.612G>T ENSP00000313397.4:p.Gln204His
ENST00000443239.7:c.486G>T ENSP00000403169.2:p.Gln162His
ENST00000456297.6:c.384G>T ENSP00000412305.1:p.Gln128His
NM_001207055.1:c.486G>T NP_001193984.1:p.Gln162His
NM_001207056.1:c.384G>T NP_001193985.1:p.Gln128His
NM_006892.3:c.612G>T , LRG_56t1:c.612G>T NP_008823.1:p.Gln204His
NM_175848.1:c.612G>T NP_787044.1:p.Gln204His
NM_175849.1:c.612G>T NP_787045.1:p.Gln204His
NM_175850.2:c.648G>T NP_787046.1:p.Gln216His
XM_011528653.1:c.648G>T XP_011526955.1:p.Gln216His
XM_011528654.1:c.522G>T XP_011526956.1:p.Gln174His
XR_936510.1:n.784G>T
XR_936511.1:n.784G>T
XR_936512.1:n.659G>T
XM_011528653.2:c.648G>T XP_011526955.1:p.Gln216His
XM_011528654.2:c.522G>T XP_011526956.1:p.Gln174His
XR_936510.2:n.795G>T
XR_936511.2:n.795G>T
XR_936512.2:n.671G>T
NM_001207055.2:c.486G>T NP_001193984.1:p.Gln162His
NM_001207056.2:c.384G>T NP_001193985.1:p.Gln128His
NM_006892.4:c.612G>T MANE Select NP_008823.1:p.Gln204His
NM_175848.2:c.612G>T NP_787044.1:p.Gln204His
NM_175849.2:c.612G>T NP_787045.1:p.Gln204His
NM_175850.3:c.648G>T NP_787046.1:p.Gln216His