Canonical Allele Identifier: CA408586488
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32787269T>A , CM000682.2:g.32787269T>A GRCh38
NC_000020.10:g.31375075T>A , CM000682.1:g.31375075T>A GRCh37
NC_000020.9:g.30838736T>A NCBI36
NG_007290.1:g.29885T>A , LRG_56:g.29885T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.472T>A ENSP00000512497.1:p.Trp158Arg
ENST00000696232.1:c.472T>A ENSP00000512498.1:p.Trp158Arg
ENST00000696233.1:c.472T>A ENSP00000512499.1:p.Trp158Arg
ENST00000696234.1:n.456T>A
ENST00000696235.1:c.346T>A ENSP00000512500.1:p.Trp116Arg
ENST00000696236.1:c.346T>A ENSP00000512501.1:p.Trp116Arg
ENST00000696237.1:n.578T>A
ENST00000696238.1:c.472T>A ENSP00000512502.1:p.Trp158Arg
ENST00000696239.1:c.472T>A ENSP00000512503.1:p.Trp158Arg
ENST00000201963.3:c.508T>A ENSP00000201963.3:p.Trp170Arg
ENST00000328111.6:c.472T>A MANE Select ENSP00000328547.2:p.Trp158Arg
ENST00000348286.6:c.472T>A ENSP00000337764.2:p.Trp158Arg
ENST00000353855.6:c.472T>A ENSP00000313397.4:p.Trp158Arg
ENST00000443239.7:c.346T>A ENSP00000403169.2:p.Trp116Arg
ENST00000456297.6:c.244T>A ENSP00000412305.1:p.Trp82Arg
NM_001207055.1:c.346T>A NP_001193984.1:p.Trp116Arg
NM_001207056.1:c.244T>A NP_001193985.1:p.Trp82Arg
NM_006892.3:c.472T>A , LRG_56t1:c.472T>A NP_008823.1:p.Trp158Arg
NM_175848.1:c.472T>A NP_787044.1:p.Trp158Arg
NM_175849.1:c.472T>A NP_787045.1:p.Trp158Arg
NM_175850.2:c.508T>A NP_787046.1:p.Trp170Arg
XM_011528653.1:c.508T>A XP_011526955.1:p.Trp170Arg
XM_011528654.1:c.382T>A XP_011526956.1:p.Trp128Arg
XR_936510.1:n.644T>A
XR_936511.1:n.644T>A
XR_936512.1:n.519T>A
XM_011528653.2:c.508T>A XP_011526955.1:p.Trp170Arg
XM_011528654.2:c.382T>A XP_011526956.1:p.Trp128Arg
XR_936510.2:n.655T>A
XR_936511.2:n.655T>A
XR_936512.2:n.531T>A
NM_001207055.2:c.346T>A NP_001193984.1:p.Trp116Arg
NM_001207056.2:c.244T>A NP_001193985.1:p.Trp82Arg
NM_006892.4:c.472T>A MANE Select NP_008823.1:p.Trp158Arg
NM_175848.2:c.472T>A NP_787044.1:p.Trp158Arg
NM_175849.2:c.472T>A NP_787045.1:p.Trp158Arg
NM_175850.3:c.508T>A NP_787046.1:p.Trp170Arg