Canonical Allele Identifier: CA2360466225
Gene: DNMT3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32807888C= , CM000682.2:g.32807888C= GRCh38
NC_000020.10:g.31395694C= , CM000682.1:g.31395694C= GRCh37
NC_000020.9:g.30859355C= NCBI36
NG_007290.1:g.50504C= , LRG_56:g.50504C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1498C= ENSP00000512497.1:n.*1498C=
ENST00000696232.1:c.2358C= ENSP00000512498.1:p.Tyr786=
ENST00000696233.1:c.*1101C= ENSP00000512499.1:n.*1101C=
ENST00000696238.1:c.*1290C= ENSP00000512502.1:n.*1290C=
ENST00000696239.1:c.2328C= ENSP00000512503.1:p.Tyr776=
ENST00000696245.1:n.572C=
ENST00000201963.3:c.2523C= ENSP00000201963.3:p.Tyr841=
ENST00000328111.6:c.2547C= MANE Select ENSP00000328547.2:p.Tyr849=
ENST00000348286.6:c.2298C= ENSP00000337764.2:p.Tyr766=
ENST00000353855.6:c.2487C= ENSP00000313397.4:p.Tyr829=
ENST00000443239.7:c.2172C= ENSP00000403169.2:p.Tyr724=
ENST00000456297.6:c.2070C= ENSP00000412305.1:p.Tyr690=
NM_001207055.1:c.2172C= NP_001193984.1:p.Tyr724=
NM_001207056.1:c.2070C= NP_001193985.1:p.Tyr690=
NM_006892.3:c.2547C= , LRG_56t1:c.2547C= NP_008823.1:p.Tyr849=
NM_175848.1:c.2487C= NP_787044.1:p.Tyr829=
NM_175849.1:c.2298C= NP_787045.1:p.Tyr766=
NM_175850.2:c.2523C= NP_787046.1:p.Tyr841=
XM_011528653.1:c.2334C= XP_011526955.1:p.Tyr778=
XM_011528654.1:c.2208C= XP_011526956.1:p.Tyr736=
XR_936511.1:n.2325C=
XM_011528653.2:c.2334C= XP_011526955.1:p.Tyr778=
XM_011528654.2:c.2208C= XP_011526956.1:p.Tyr736=
XR_936511.2:n.2336C=
NM_001207055.2:c.2172C= NP_001193984.1:p.Tyr724=
NM_001207056.2:c.2070C= NP_001193985.1:p.Tyr690=
NM_006892.4:c.2547C= MANE Select NP_008823.1:p.Tyr849=
NM_175848.2:c.2487C= NP_787044.1:p.Tyr829=
NM_175849.2:c.2298C= NP_787045.1:p.Tyr766=
NM_175850.3:c.2523C= NP_787046.1:p.Tyr841=