Canonical Allele Identifier: CA2360465140
Gene: DNMT3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32805372C= , CM000682.2:g.32805372C= GRCh38
NC_000020.10:g.31393178C= , CM000682.1:g.31393178C= GRCh37
NC_000020.9:g.30856839C= NCBI36
NG_007290.1:g.47988C= , LRG_56:g.47988C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1217C= ENSP00000512497.1:n.*1217C=
ENST00000696232.1:c.2232-2390C= ENSP00000512498.1:n.2232-2390C=
ENST00000696233.1:c.*975-2390C= ENSP00000512499.1:n.*975-2390C=
ENST00000696238.1:c.*1009C= ENSP00000512502.1:n.*1009C=
ENST00000696239.1:c.2047C= ENSP00000512503.1:p.Leu683=
ENST00000696245.1:n.327-837C=
ENST00000201963.3:c.2242C= ENSP00000201963.3:p.Leu748=
ENST00000328111.6:c.2266C= MANE Select ENSP00000328547.2:p.Leu756=
ENST00000348286.6:c.2172-2390C= ENSP00000337764.2:n.2172-2390C=
ENST00000353855.6:c.2206C= ENSP00000313397.4:p.Leu736=
ENST00000443239.7:c.2046-2390C= ENSP00000403169.2:n.2046-2390C=
ENST00000456297.6:c.1944-2390C= ENSP00000412305.1:n.1944-2390C=
NM_001207055.1:c.2046-2390C= NP_001193984.1:n.2046-2390C=
NM_001207056.1:c.1944-2390C= NP_001193985.1:n.1944-2390C=
NM_006892.3:c.2266C= , LRG_56t1:c.2266C= NP_008823.1:p.Leu756=
NM_175848.1:c.2206C= NP_787044.1:p.Leu736=
NM_175849.1:c.2172-2390C= NP_787045.1:n.2172-2390C=
NM_175850.2:c.2242C= NP_787046.1:p.Leu748=
XM_011528653.1:c.2208-2390C= XP_011526955.1:n.2208-2390C=
XM_011528654.1:c.2082-2390C= XP_011526956.1:n.2082-2390C=
XR_936510.1:n.2233C=
XR_936511.1:n.2199-2390C=
XR_936512.1:n.2108C=
XM_011528653.2:c.2208-2390C= XP_011526955.1:n.2208-2390C=
XM_011528654.2:c.2082-2390C= XP_011526956.1:n.2082-2390C=
XR_936510.2:n.2244C=
XR_936511.2:n.2210-2390C=
XR_936512.2:n.2120C=
NM_001207055.2:c.2046-2390C= NP_001193984.1:n.2046-2390C=
NM_001207056.2:c.1944-2390C= NP_001193985.1:n.1944-2390C=
NM_006892.4:c.2266C= MANE Select NP_008823.1:p.Leu756=
NM_175848.2:c.2206C= NP_787044.1:p.Leu736=
NM_175849.2:c.2172-2390C= NP_787045.1:n.2172-2390C=
NM_175850.3:c.2242C= NP_787046.1:p.Leu748=