Canonical Allele Identifier: CA2360466296
Gene: DNMT3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32808015C= , CM000682.2:g.32808015C= GRCh38
NC_000020.10:g.31395821C= , CM000682.1:g.31395821C= GRCh37
NC_000020.9:g.30859482C= NCBI36
NG_007290.1:g.50631C= , LRG_56:g.50631C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1625C= ENSP00000512497.1:n.*1625C=
ENST00000696232.1:c.*112C= ENSP00000512498.1:n.*112C=
ENST00000696233.1:c.*1228C= ENSP00000512499.1:n.*1228C=
ENST00000696238.1:c.*1417C= ENSP00000512502.1:n.*1417C=
ENST00000696245.1:n.699C=
ENST00000201963.3:c.*112C= ENSP00000201963.3:n.*112C=
ENST00000328111.6:c.*112C= MANE Select ENSP00000328547.2:n.*112C=
ENST00000348286.6:c.*112C= ENSP00000337764.2:n.*112C=
ENST00000353855.6:c.*112C= ENSP00000313397.4:n.*112C=
ENST00000443239.7:c.*112C= ENSP00000403169.2:n.*112C=
ENST00000456297.6:c.*112C= ENSP00000412305.1:n.*112C=
NM_001207055.1:c.*112C= NP_001193984.1:n.*112C=
NM_001207056.1:c.*112C= NP_001193985.1:n.*112C=
NM_006892.3:c.*112C= , LRG_56t1:c.*112C= NP_008823.1:n.*112C=
NM_175848.1:c.*112C= NP_787044.1:n.*112C=
NM_175849.1:c.*112C= NP_787045.1:n.*112C=
NM_175850.2:c.*112C= NP_787046.1:n.*112C=
XM_011528653.1:c.*112C= XP_011526955.1:n.*112C=
XM_011528654.1:c.*112C= XP_011526956.1:n.*112C=
XR_936511.1:n.2452C=
XM_011528653.2:c.*112C= XP_011526955.1:n.*112C=
XM_011528654.2:c.*112C= XP_011526956.1:n.*112C=
XR_936511.2:n.2463C=
NM_001207055.2:c.*112C= NP_001193984.1:n.*112C=
NM_001207056.2:c.*112C= NP_001193985.1:n.*112C=
NM_006892.4:c.*112C= MANE Select NP_008823.1:n.*112C=
NM_175848.2:c.*112C= NP_787044.1:n.*112C=
NM_175849.2:c.*112C= NP_787045.1:n.*112C=
NM_175850.3:c.*112C= NP_787046.1:n.*112C=