Canonical Allele Identifier: CA2360465125
Gene: DNMT3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32805341C= , CM000682.2:g.32805341C= GRCh38
NC_000020.10:g.31393147C= , CM000682.1:g.31393147C= GRCh37
NC_000020.9:g.30856808C= NCBI36
NG_007290.1:g.47957C= , LRG_56:g.47957C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1186C= ENSP00000512497.1:n.*1186C=
ENST00000696232.1:c.2232-2421C= ENSP00000512498.1:n.2232-2421C=
ENST00000696233.1:c.*975-2421C= ENSP00000512499.1:n.*975-2421C=
ENST00000696238.1:c.*978C= ENSP00000512502.1:n.*978C=
ENST00000696239.1:c.2016C= ENSP00000512503.1:p.Pro672=
ENST00000696245.1:n.327-868C=
ENST00000201963.3:c.2211C= ENSP00000201963.3:p.Pro737=
ENST00000328111.6:c.2235C= MANE Select ENSP00000328547.2:p.Pro745=
ENST00000348286.6:c.2172-2421C= ENSP00000337764.2:n.2172-2421C=
ENST00000353855.6:c.2175C= ENSP00000313397.4:p.Pro725=
ENST00000443239.7:c.2046-2421C= ENSP00000403169.2:n.2046-2421C=
ENST00000456297.6:c.1944-2421C= ENSP00000412305.1:n.1944-2421C=
NM_001207055.1:c.2046-2421C= NP_001193984.1:n.2046-2421C=
NM_001207056.1:c.1944-2421C= NP_001193985.1:n.1944-2421C=
NM_006892.3:c.2235C= , LRG_56t1:c.2235C= NP_008823.1:p.Pro745=
NM_175848.1:c.2175C= NP_787044.1:p.Pro725=
NM_175849.1:c.2172-2421C= NP_787045.1:n.2172-2421C=
NM_175850.2:c.2211C= NP_787046.1:p.Pro737=
XM_011528653.1:c.2208-2421C= XP_011526955.1:n.2208-2421C=
XM_011528654.1:c.2082-2421C= XP_011526956.1:n.2082-2421C=
XR_936510.1:n.2202C=
XR_936511.1:n.2199-2421C=
XR_936512.1:n.2077C=
XM_011528653.2:c.2208-2421C= XP_011526955.1:n.2208-2421C=
XM_011528654.2:c.2082-2421C= XP_011526956.1:n.2082-2421C=
XR_936510.2:n.2213C=
XR_936511.2:n.2210-2421C=
XR_936512.2:n.2089C=
NM_001207055.2:c.2046-2421C= NP_001193984.1:n.2046-2421C=
NM_001207056.2:c.1944-2421C= NP_001193985.1:n.1944-2421C=
NM_006892.4:c.2235C= MANE Select NP_008823.1:p.Pro745=
NM_175848.2:c.2175C= NP_787044.1:p.Pro725=
NM_175849.2:c.2172-2421C= NP_787045.1:n.2172-2421C=
NM_175850.3:c.2211C= NP_787046.1:p.Pro737=