Canonical Allele Identifier: CA2360465145
Gene: DNMT3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32805386G= , CM000682.2:g.32805386G= GRCh38
NC_000020.10:g.31393192G= , CM000682.1:g.31393192G= GRCh37
NC_000020.9:g.30856853G= NCBI36
NG_007290.1:g.48002G= , LRG_56:g.48002G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1231G= ENSP00000512497.1:n.*1231G=
ENST00000696232.1:c.2232-2376G= ENSP00000512498.1:n.2232-2376G=
ENST00000696233.1:c.*975-2376G= ENSP00000512499.1:n.*975-2376G=
ENST00000696238.1:c.*1023G= ENSP00000512502.1:n.*1023G=
ENST00000696239.1:c.2061G= ENSP00000512503.1:p.Leu687=
ENST00000696245.1:n.327-823G=
ENST00000201963.3:c.2256G= ENSP00000201963.3:p.Leu752=
ENST00000328111.6:c.2280G= MANE Select ENSP00000328547.2:p.Leu760=
ENST00000348286.6:c.2172-2376G= ENSP00000337764.2:n.2172-2376G=
ENST00000353855.6:c.2220G= ENSP00000313397.4:p.Leu740=
ENST00000443239.7:c.2046-2376G= ENSP00000403169.2:n.2046-2376G=
ENST00000456297.6:c.1944-2376G= ENSP00000412305.1:n.1944-2376G=
NM_001207055.1:c.2046-2376G= NP_001193984.1:n.2046-2376G=
NM_001207056.1:c.1944-2376G= NP_001193985.1:n.1944-2376G=
NM_006892.3:c.2280G= , LRG_56t1:c.2280G= NP_008823.1:p.Leu760=
NM_175848.1:c.2220G= NP_787044.1:p.Leu740=
NM_175849.1:c.2172-2376G= NP_787045.1:n.2172-2376G=
NM_175850.2:c.2256G= NP_787046.1:p.Leu752=
XM_011528653.1:c.2208-2376G= XP_011526955.1:n.2208-2376G=
XM_011528654.1:c.2082-2376G= XP_011526956.1:n.2082-2376G=
XR_936510.1:n.2247G=
XR_936511.1:n.2199-2376G=
XR_936512.1:n.2122G=
XM_011528653.2:c.2208-2376G= XP_011526955.1:n.2208-2376G=
XM_011528654.2:c.2082-2376G= XP_011526956.1:n.2082-2376G=
XR_936510.2:n.2258G=
XR_936511.2:n.2210-2376G=
XR_936512.2:n.2134G=
NM_001207055.2:c.2046-2376G= NP_001193984.1:n.2046-2376G=
NM_001207056.2:c.1944-2376G= NP_001193985.1:n.1944-2376G=
NM_006892.4:c.2280G= MANE Select NP_008823.1:p.Leu760=
NM_175848.2:c.2220G= NP_787044.1:p.Leu740=
NM_175849.2:c.2172-2376G= NP_787045.1:n.2172-2376G=
NM_175850.3:c.2256G= NP_787046.1:p.Leu752=