Canonical Allele Identifier: CA4847648
Gene: SYBU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109575975C>T , CM000670.2:g.109575975C>T GRCh38
NC_000008.10:g.110588204C>T , CM000670.1:g.110588204C>T GRCh37
NC_000008.9:g.110657380C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000276646.14:c.923G>A MANE Select ENSP00000276646.9:p.Arg308His
ENST00000276646.13:c.923G>A ENSP00000276646.9:p.Arg308His
ENST00000399066.7:c.914G>A ENSP00000382019.3:p.Arg305His
ENST00000408889.7:c.566G>A ENSP00000386196.3:p.Arg189His
ENST00000408908.6:c.923G>A ENSP00000386154.2:p.Arg308His
ENST00000422135.5:c.923G>A ENSP00000407118.1:p.Arg308His
ENST00000424158.6:c.938G>A ENSP00000415654.2:p.Arg313His
ENST00000433638.1:c.923G>A ENSP00000403544.1:p.Arg308His
ENST00000440310.5:c.923G>A ENSP00000404369.1:p.Arg308His
ENST00000446070.6:c.920G>A ENSP00000414748.2:p.Arg307His
ENST00000527707.5:n.573G>A
ENST00000528331.5:c.566G>A ENSP00000436041.1:p.Arg189His
ENST00000528647.5:c.920G>A ENSP00000432501.1:p.Arg307His
ENST00000529175.5:c.305G>A ENSP00000434871.1:p.Arg102His
ENST00000529690.5:c.533G>A ENSP00000433941.1:p.Arg178His
ENST00000532779.5:c.719G>A ENSP00000436266.1:p.Arg240His
ENST00000533065.5:c.566G>A ENSP00000432962.1:p.Arg189His
ENST00000533171.5:c.923G>A ENSP00000434679.1:p.Arg308His
ENST00000533394.5:c.434G>A
ENST00000533895.5:c.920G>A ENSP00000433446.1:p.Arg307His
NM_001099743.1:c.920G>A NP_001093213.1:p.Arg307His
NM_001099744.1:c.923G>A NP_001093214.1:p.Arg308His
NM_001099745.1:c.923G>A NP_001093215.1:p.Arg308His
NM_001099746.1:c.566G>A NP_001093216.1:p.Arg189His
NM_001099747.1:c.920G>A NP_001093217.1:p.Arg307His
NM_001099748.1:c.923G>A NP_001093218.1:p.Arg308His
NM_001099749.1:c.566G>A NP_001093219.1:p.Arg189His
NM_001099750.1:c.923G>A NP_001093220.1:p.Arg308His
NM_001099751.1:c.920G>A NP_001093221.1:p.Arg307His
NM_001099752.1:c.923G>A NP_001093222.1:p.Arg308His
NM_001099753.1:c.920G>A NP_001093223.1:p.Arg307His
NM_001099754.1:c.923G>A NP_001093224.1:p.Arg308His
NM_001099755.1:c.566G>A NP_001093225.1:p.Arg189His
NM_001099756.1:c.914G>A NP_001093226.1:p.Arg305His
NM_017786.5:c.920G>A NP_060256.3:p.Arg307His
XM_005250999.1:c.533G>A XP_005251056.1:p.Arg178His
XM_005251000.1:c.434G>A XP_005251057.1:p.Arg145His
XM_011517154.1:c.422G>A XP_011515456.1:p.Arg141His
NM_001330596.1:c.533G>A NP_001317525.1:p.Arg178His
NM_001363032.1:c.434G>A NP_001349961.1:p.Arg145His
XM_011517154.2:c.422G>A XP_011515456.1:p.Arg141His
XM_017013614.1:c.566G>A XP_016869103.1:p.Arg189His
XM_017013615.1:c.566G>A XP_016869104.1:p.Arg189His
NM_001099754.2:c.923G>A MANE Select NP_001093224.1:p.Arg308His
NM_001099743.2:c.920G>A NP_001093213.1:p.Arg307His
NM_001099745.2:c.923G>A NP_001093215.1:p.Arg308His
NM_001099747.2:c.920G>A NP_001093217.1:p.Arg307His
NM_001099749.2:c.566G>A NP_001093219.1:p.Arg189His
NM_001099753.2:c.920G>A NP_001093223.1:p.Arg307His
NM_001099755.2:c.566G>A NP_001093225.1:p.Arg189His
NM_001330596.2:c.533G>A NP_001317525.1:p.Arg178His
NM_001363032.2:c.434G>A NP_001349961.1:p.Arg145His
NM_017786.6:c.920G>A NP_060256.3:p.Arg307His
NM_001099744.2:c.923G>A NP_001093214.1:p.Arg308His
NM_001099746.2:c.566G>A NP_001093216.1:p.Arg189His
NM_001099748.2:c.923G>A NP_001093218.1:p.Arg308His
NM_001099750.2:c.923G>A NP_001093220.1:p.Arg308His
NM_001099751.2:c.920G>A NP_001093221.1:p.Arg307His
NM_001099752.2:c.923G>A NP_001093222.1:p.Arg308His