Canonical Allele Identifier: CA408588483
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32800258T>A , CM000682.2:g.32800258T>A GRCh38
NC_000020.10:g.31388064T>A , CM000682.1:g.31388064T>A GRCh37
NC_000020.9:g.30851725T>A NCBI36
NG_007290.1:g.42874T>A , LRG_56:g.42874T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*816T>A ENSP00000512497.1:n.*816T>A
ENST00000696232.1:c.1865T>A ENSP00000512498.1:p.Ile622Asn
ENST00000696233.1:c.*608T>A ENSP00000512499.1:n.*608T>A
ENST00000696235.1:c.*513T>A ENSP00000512500.1:n.*513T>A
ENST00000696238.1:c.*608T>A ENSP00000512502.1:n.*608T>A
ENST00000696239.1:c.1646T>A ENSP00000512503.1:p.Ile549Asn
ENST00000201963.3:c.1841T>A ENSP00000201963.3:p.Ile614Asn
ENST00000328111.6:c.1865T>A MANE Select ENSP00000328547.2:p.Ile622Asn
ENST00000348286.6:c.1805T>A ENSP00000337764.2:p.Ile602Asn
ENST00000353855.6:c.1805T>A ENSP00000313397.4:p.Ile602Asn
ENST00000443239.7:c.1679T>A ENSP00000403169.2:p.Ile560Asn
ENST00000456297.6:c.1577T>A ENSP00000412305.1:p.Ile526Asn
NM_001207055.1:c.1679T>A NP_001193984.1:p.Ile560Asn
NM_001207056.1:c.1577T>A NP_001193985.1:p.Ile526Asn
NM_006892.3:c.1865T>A , LRG_56t1:c.1865T>A NP_008823.1:p.Ile622Asn
NM_175848.1:c.1805T>A NP_787044.1:p.Ile602Asn
NM_175849.1:c.1805T>A NP_787045.1:p.Ile602Asn
NM_175850.2:c.1841T>A NP_787046.1:p.Ile614Asn
XM_011528653.1:c.1841T>A XP_011526955.1:p.Ile614Asn
XM_011528654.1:c.1715T>A XP_011526956.1:p.Ile572Asn
XR_936510.1:n.1832T>A
XR_936511.1:n.1832T>A
XR_936512.1:n.1707T>A
XM_011528653.2:c.1841T>A XP_011526955.1:p.Ile614Asn
XM_011528654.2:c.1715T>A XP_011526956.1:p.Ile572Asn
XR_936510.2:n.1843T>A
XR_936511.2:n.1843T>A
XR_936512.2:n.1719T>A
NM_001207055.2:c.1679T>A NP_001193984.1:p.Ile560Asn
NM_001207056.2:c.1577T>A NP_001193985.1:p.Ile526Asn
NM_006892.4:c.1865T>A MANE Select NP_008823.1:p.Ile622Asn
NM_175848.2:c.1805T>A NP_787044.1:p.Ile602Asn
NM_175849.2:c.1805T>A NP_787045.1:p.Ile602Asn
NM_175850.3:c.1841T>A NP_787046.1:p.Ile614Asn