Canonical Allele Identifier: CA408588454
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32800245C>A , CM000682.2:g.32800245C>A GRCh38
NC_000020.10:g.31388051C>A , CM000682.1:g.31388051C>A GRCh37
NC_000020.9:g.30851712C>A NCBI36
NG_007290.1:g.42861C>A , LRG_56:g.42861C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*803C>A ENSP00000512497.1:n.*803C>A
ENST00000696232.1:c.1852C>A ENSP00000512498.1:p.His618Asn
ENST00000696233.1:c.*595C>A ENSP00000512499.1:n.*595C>A
ENST00000696235.1:c.*500C>A ENSP00000512500.1:n.*500C>A
ENST00000696238.1:c.*595C>A ENSP00000512502.1:n.*595C>A
ENST00000696239.1:c.1633C>A ENSP00000512503.1:p.His545Asn
ENST00000201963.3:c.1828C>A ENSP00000201963.3:p.His610Asn
ENST00000328111.6:c.1852C>A MANE Select ENSP00000328547.2:p.His618Asn
ENST00000348286.6:c.1792C>A ENSP00000337764.2:p.His598Asn
ENST00000353855.6:c.1792C>A ENSP00000313397.4:p.His598Asn
ENST00000443239.7:c.1666C>A ENSP00000403169.2:p.His556Asn
ENST00000456297.6:c.1564C>A ENSP00000412305.1:p.His522Asn
NM_001207055.1:c.1666C>A NP_001193984.1:p.His556Asn
NM_001207056.1:c.1564C>A NP_001193985.1:p.His522Asn
NM_006892.3:c.1852C>A , LRG_56t1:c.1852C>A NP_008823.1:p.His618Asn
NM_175848.1:c.1792C>A NP_787044.1:p.His598Asn
NM_175849.1:c.1792C>A NP_787045.1:p.His598Asn
NM_175850.2:c.1828C>A NP_787046.1:p.His610Asn
XM_011528653.1:c.1828C>A XP_011526955.1:p.His610Asn
XM_011528654.1:c.1702C>A XP_011526956.1:p.His568Asn
XR_936510.1:n.1819C>A
XR_936511.1:n.1819C>A
XR_936512.1:n.1694C>A
XM_011528653.2:c.1828C>A XP_011526955.1:p.His610Asn
XM_011528654.2:c.1702C>A XP_011526956.1:p.His568Asn
XR_936510.2:n.1830C>A
XR_936511.2:n.1830C>A
XR_936512.2:n.1706C>A
NM_001207055.2:c.1666C>A NP_001193984.1:p.His556Asn
NM_001207056.2:c.1564C>A NP_001193985.1:p.His522Asn
NM_006892.4:c.1852C>A MANE Select NP_008823.1:p.His618Asn
NM_175848.2:c.1792C>A NP_787044.1:p.His598Asn
NM_175849.2:c.1792C>A NP_787045.1:p.His598Asn
NM_175850.3:c.1828C>A NP_787046.1:p.His610Asn