Canonical Allele Identifier: CA408588505
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32800269A>T , CM000682.2:g.32800269A>T GRCh38
NC_000020.10:g.31388075A>T , CM000682.1:g.31388075A>T GRCh37
NC_000020.9:g.30851736A>T NCBI36
NG_007290.1:g.42885A>T , LRG_56:g.42885A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*827A>T ENSP00000512497.1:n.*827A>T
ENST00000696232.1:c.1876A>T ENSP00000512498.1:p.Asn626Tyr
ENST00000696233.1:c.*619A>T ENSP00000512499.1:n.*619A>T
ENST00000696235.1:c.*524A>T ENSP00000512500.1:n.*524A>T
ENST00000696238.1:c.*619A>T ENSP00000512502.1:n.*619A>T
ENST00000696239.1:c.1657A>T ENSP00000512503.1:p.Asn553Tyr
ENST00000201963.3:c.1852A>T ENSP00000201963.3:p.Asn618Tyr
ENST00000328111.6:c.1876A>T MANE Select ENSP00000328547.2:p.Asn626Tyr
ENST00000348286.6:c.1816A>T ENSP00000337764.2:p.Asn606Tyr
ENST00000353855.6:c.1816A>T ENSP00000313397.4:p.Asn606Tyr
ENST00000443239.7:c.1690A>T ENSP00000403169.2:p.Asn564Tyr
ENST00000456297.6:c.1588A>T ENSP00000412305.1:p.Asn530Tyr
NM_001207055.1:c.1690A>T NP_001193984.1:p.Asn564Tyr
NM_001207056.1:c.1588A>T NP_001193985.1:p.Asn530Tyr
NM_006892.3:c.1876A>T , LRG_56t1:c.1876A>T NP_008823.1:p.Asn626Tyr
NM_175848.1:c.1816A>T NP_787044.1:p.Asn606Tyr
NM_175849.1:c.1816A>T NP_787045.1:p.Asn606Tyr
NM_175850.2:c.1852A>T NP_787046.1:p.Asn618Tyr
XM_011528653.1:c.1852A>T XP_011526955.1:p.Asn618Tyr
XM_011528654.1:c.1726A>T XP_011526956.1:p.Asn576Tyr
XR_936510.1:n.1843A>T
XR_936511.1:n.1843A>T
XR_936512.1:n.1718A>T
XM_011528653.2:c.1852A>T XP_011526955.1:p.Asn618Tyr
XM_011528654.2:c.1726A>T XP_011526956.1:p.Asn576Tyr
XR_936510.2:n.1854A>T
XR_936511.2:n.1854A>T
XR_936512.2:n.1730A>T
NM_001207055.2:c.1690A>T NP_001193984.1:p.Asn564Tyr
NM_001207056.2:c.1588A>T NP_001193985.1:p.Asn530Tyr
NM_006892.4:c.1876A>T MANE Select NP_008823.1:p.Asn626Tyr
NM_175848.2:c.1816A>T NP_787044.1:p.Asn606Tyr
NM_175849.2:c.1816A>T NP_787045.1:p.Asn606Tyr
NM_175850.3:c.1852A>T NP_787046.1:p.Asn618Tyr