Canonical Allele Identifier: CA408586952
Gene: DNMT3B HGNC NCBI

Linked Data

dbSNP Id: rs1278887797

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32787422A>C , CM000682.2:g.32787422A>C GRCh38
NC_000020.10:g.31375228A>C , CM000682.1:g.31375228A>C GRCh37
NC_000020.9:g.30838889A>C NCBI36
NG_007290.1:g.30038A>C , LRG_56:g.30038A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.625A>C ENSP00000512497.1:p.Ser209Arg
ENST00000696232.1:c.625A>C ENSP00000512498.1:p.Ser209Arg
ENST00000696233.1:c.625A>C ENSP00000512499.1:p.Ser209Arg
ENST00000696234.1:n.609A>C
ENST00000696235.1:c.499A>C ENSP00000512500.1:p.Ser167Arg
ENST00000696236.1:c.499A>C ENSP00000512501.1:p.Ser167Arg
ENST00000696237.1:n.731A>C
ENST00000696238.1:c.625A>C ENSP00000512502.1:p.Ser209Arg
ENST00000696239.1:c.625A>C ENSP00000512503.1:p.Ser209Arg
ENST00000201963.3:c.661A>C ENSP00000201963.3:p.Ser221Arg
ENST00000328111.6:c.625A>C MANE Select ENSP00000328547.2:p.Ser209Arg
ENST00000348286.6:c.625A>C ENSP00000337764.2:p.Ser209Arg
ENST00000353855.6:c.625A>C ENSP00000313397.4:p.Ser209Arg
ENST00000443239.7:c.499A>C ENSP00000403169.2:p.Ser167Arg
ENST00000456297.6:c.397A>C ENSP00000412305.1:p.Ser133Arg
NM_001207055.1:c.499A>C NP_001193984.1:p.Ser167Arg
NM_001207056.1:c.397A>C NP_001193985.1:p.Ser133Arg
NM_006892.3:c.625A>C , LRG_56t1:c.625A>C NP_008823.1:p.Ser209Arg
NM_175848.1:c.625A>C NP_787044.1:p.Ser209Arg
NM_175849.1:c.625A>C NP_787045.1:p.Ser209Arg
NM_175850.2:c.661A>C NP_787046.1:p.Ser221Arg
XM_011528653.1:c.661A>C XP_011526955.1:p.Ser221Arg
XM_011528654.1:c.535A>C XP_011526956.1:p.Ser179Arg
XR_936510.1:n.797A>C
XR_936511.1:n.797A>C
XR_936512.1:n.672A>C
XM_011528653.2:c.661A>C XP_011526955.1:p.Ser221Arg
XM_011528654.2:c.535A>C XP_011526956.1:p.Ser179Arg
XR_936510.2:n.808A>C
XR_936511.2:n.808A>C
XR_936512.2:n.684A>C
NM_001207055.2:c.499A>C NP_001193984.1:p.Ser167Arg
NM_001207056.2:c.397A>C NP_001193985.1:p.Ser133Arg
NM_006892.4:c.625A>C MANE Select NP_008823.1:p.Ser209Arg
NM_175848.2:c.625A>C NP_787044.1:p.Ser209Arg
NM_175849.2:c.625A>C NP_787045.1:p.Ser209Arg
NM_175850.3:c.661A>C NP_787046.1:p.Ser221Arg