Canonical Allele Identifier: CA408588500
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32800267T>A , CM000682.2:g.32800267T>A GRCh38
NC_000020.10:g.31388073T>A , CM000682.1:g.31388073T>A GRCh37
NC_000020.9:g.30851734T>A NCBI36
NG_007290.1:g.42883T>A , LRG_56:g.42883T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*825T>A ENSP00000512497.1:n.*825T>A
ENST00000696232.1:c.1874T>A ENSP00000512498.1:p.Val625Glu
ENST00000696233.1:c.*617T>A ENSP00000512499.1:n.*617T>A
ENST00000696235.1:c.*522T>A ENSP00000512500.1:n.*522T>A
ENST00000696238.1:c.*617T>A ENSP00000512502.1:n.*617T>A
ENST00000696239.1:c.1655T>A ENSP00000512503.1:p.Val552Glu
ENST00000201963.3:c.1850T>A ENSP00000201963.3:p.Val617Glu
ENST00000328111.6:c.1874T>A MANE Select ENSP00000328547.2:p.Val625Glu
ENST00000348286.6:c.1814T>A ENSP00000337764.2:p.Val605Glu
ENST00000353855.6:c.1814T>A ENSP00000313397.4:p.Val605Glu
ENST00000443239.7:c.1688T>A ENSP00000403169.2:p.Val563Glu
ENST00000456297.6:c.1586T>A ENSP00000412305.1:p.Val529Glu
NM_001207055.1:c.1688T>A NP_001193984.1:p.Val563Glu
NM_001207056.1:c.1586T>A NP_001193985.1:p.Val529Glu
NM_006892.3:c.1874T>A , LRG_56t1:c.1874T>A NP_008823.1:p.Val625Glu
NM_175848.1:c.1814T>A NP_787044.1:p.Val605Glu
NM_175849.1:c.1814T>A NP_787045.1:p.Val605Glu
NM_175850.2:c.1850T>A NP_787046.1:p.Val617Glu
XM_011528653.1:c.1850T>A XP_011526955.1:p.Val617Glu
XM_011528654.1:c.1724T>A XP_011526956.1:p.Val575Glu
XR_936510.1:n.1841T>A
XR_936511.1:n.1841T>A
XR_936512.1:n.1716T>A
XM_011528653.2:c.1850T>A XP_011526955.1:p.Val617Glu
XM_011528654.2:c.1724T>A XP_011526956.1:p.Val575Glu
XR_936510.2:n.1852T>A
XR_936511.2:n.1852T>A
XR_936512.2:n.1728T>A
NM_001207055.2:c.1688T>A NP_001193984.1:p.Val563Glu
NM_001207056.2:c.1586T>A NP_001193985.1:p.Val529Glu
NM_006892.4:c.1874T>A MANE Select NP_008823.1:p.Val625Glu
NM_175848.2:c.1814T>A NP_787044.1:p.Val605Glu
NM_175849.2:c.1814T>A NP_787045.1:p.Val605Glu
NM_175850.3:c.1850T>A NP_787046.1:p.Val617Glu