Canonical Allele Identifier: CA408593108
Gene: DNMT3B HGNC NCBI

Linked Data

dbSNP Id: rs955772228

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32807846C>A , CM000682.2:g.32807846C>A GRCh38
NC_000020.10:g.31395652C>A , CM000682.1:g.31395652C>A GRCh37
NC_000020.9:g.30859313C>A NCBI36
NG_007290.1:g.50462C>A , LRG_56:g.50462C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1456C>A ENSP00000512497.1:n.*1456C>A
ENST00000696232.1:c.2316C>A ENSP00000512498.1:p.Ser772Arg
ENST00000696233.1:c.*1059C>A ENSP00000512499.1:n.*1059C>A
ENST00000696238.1:c.*1248C>A ENSP00000512502.1:n.*1248C>A
ENST00000696239.1:c.2286C>A ENSP00000512503.1:p.Ser762Arg
ENST00000696245.1:n.530C>A
ENST00000201963.3:c.2481C>A ENSP00000201963.3:p.Ser827Arg
ENST00000328111.6:c.2505C>A MANE Select ENSP00000328547.2:p.Ser835Arg
ENST00000348286.6:c.2256C>A ENSP00000337764.2:p.Ser752Arg
ENST00000353855.6:c.2445C>A ENSP00000313397.4:p.Ser815Arg
ENST00000443239.7:c.2130C>A ENSP00000403169.2:p.Ser710Arg
ENST00000456297.6:c.2028C>A ENSP00000412305.1:p.Ser676Arg
NM_001207055.1:c.2130C>A NP_001193984.1:p.Ser710Arg
NM_001207056.1:c.2028C>A NP_001193985.1:p.Ser676Arg
NM_006892.3:c.2505C>A , LRG_56t1:c.2505C>A NP_008823.1:p.Ser835Arg
NM_175848.1:c.2445C>A NP_787044.1:p.Ser815Arg
NM_175849.1:c.2256C>A NP_787045.1:p.Ser752Arg
NM_175850.2:c.2481C>A NP_787046.1:p.Ser827Arg
XM_011528653.1:c.2292C>A XP_011526955.1:p.Ser764Arg
XM_011528654.1:c.2166C>A XP_011526956.1:p.Ser722Arg
XR_936511.1:n.2283C>A
XM_011528653.2:c.2292C>A XP_011526955.1:p.Ser764Arg
XM_011528654.2:c.2166C>A XP_011526956.1:p.Ser722Arg
XR_936511.2:n.2294C>A
NM_001207055.2:c.2130C>A NP_001193984.1:p.Ser710Arg
NM_001207056.2:c.2028C>A NP_001193985.1:p.Ser676Arg
NM_006892.4:c.2505C>A MANE Select NP_008823.1:p.Ser835Arg
NM_175848.2:c.2445C>A NP_787044.1:p.Ser815Arg
NM_175849.2:c.2256C>A NP_787045.1:p.Ser752Arg
NM_175850.3:c.2481C>A NP_787046.1:p.Ser827Arg