Canonical Allele Identifier: CA510212022
Gene: DNMT3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.31393177G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32805371G>A , CM000682.2:g.32805371G>A GRCh38
NC_000020.10:g.31393177G>A , CM000682.1:g.31393177G>A GRCh37
NC_000020.9:g.30856838G>A NCBI36
NG_007290.1:g.47987G>A , LRG_56:g.47987G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1216G>A ENSP00000512497.1:n.*1216G>A
ENST00000696232.1:c.2232-2391G>A ENSP00000512498.1:n.2232-2391G>A
ENST00000696233.1:c.*975-2391G>A ENSP00000512499.1:n.*975-2391G>A
ENST00000696238.1:c.*1008G>A ENSP00000512502.1:n.*1008G>A
ENST00000696239.1:c.2046G>A ENSP00000512503.1:p.Glu682=
ENST00000696245.1:n.327-838G>A
ENST00000201963.3:c.2241G>A ENSP00000201963.3:p.Glu747=
ENST00000328111.6:c.2265G>A MANE Select ENSP00000328547.2:p.Glu755=
ENST00000348286.6:c.2172-2391G>A ENSP00000337764.2:n.2172-2391G>A
ENST00000353855.6:c.2205G>A ENSP00000313397.4:p.Glu735=
ENST00000443239.7:c.2046-2391G>A ENSP00000403169.2:n.2046-2391G>A
ENST00000456297.6:c.1944-2391G>A ENSP00000412305.1:n.1944-2391G>A
NM_001207055.1:c.2046-2391G>A NP_001193984.1:n.2046-2391G>A
NM_001207056.1:c.1944-2391G>A NP_001193985.1:n.1944-2391G>A
NM_006892.3:c.2265G>A , LRG_56t1:c.2265G>A NP_008823.1:p.Glu755=
NM_175848.1:c.2205G>A NP_787044.1:p.Glu735=
NM_175849.1:c.2172-2391G>A NP_787045.1:n.2172-2391G>A
NM_175850.2:c.2241G>A NP_787046.1:p.Glu747=
XM_011528653.1:c.2208-2391G>A XP_011526955.1:n.2208-2391G>A
XM_011528654.1:c.2082-2391G>A XP_011526956.1:n.2082-2391G>A
XR_936510.1:n.2232G>A
XR_936511.1:n.2199-2391G>A
XR_936512.1:n.2107G>A
XM_011528653.2:c.2208-2391G>A XP_011526955.1:n.2208-2391G>A
XM_011528654.2:c.2082-2391G>A XP_011526956.1:n.2082-2391G>A
XR_936510.2:n.2243G>A
XR_936511.2:n.2210-2391G>A
XR_936512.2:n.2119G>A
NM_001207055.2:c.2046-2391G>A NP_001193984.1:n.2046-2391G>A
NM_001207056.2:c.1944-2391G>A NP_001193985.1:n.1944-2391G>A
NM_006892.4:c.2265G>A MANE Select NP_008823.1:p.Glu755=
NM_175848.2:c.2205G>A NP_787044.1:p.Glu735=
NM_175849.2:c.2172-2391G>A NP_787045.1:n.2172-2391G>A
NM_175850.3:c.2241G>A NP_787046.1:p.Glu747=