Canonical Allele Identifier: CA1584036780

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371315A= , CM000667.2:g.134371315A= GRCh38
NC_000005.9:g.133707006A= , CM000667.1:g.133707006A= GRCh37
NC_000005.8:g.133734905A= NCBI36
NG_042179.2:g.4733T=
NG_046936.1:g.5140A=

Transcript Alleles

HGVS Amino-acid change
ENST00000507277.2:c.-281A= (UBE2B) ENSP00000425137.2:n.-281A=
ENST00000265339.6:c.-281A= (UBE2B) ENSP00000265339.2:n.-281A=
NM_003337.3:c.-281A= (UBE2B) NP_003328.1:n.-281A=
XM_011543441.1:c.-224+83T= (CDKL3) XP_011541743.1:n.-224+83T=
XM_017009544.2:c.-949T= (CDKL3) XP_016865033.1:n.-949T=
XM_017009545.2:c.-754T= (CDKL3) XP_016865034.1:n.-754T=
XM_024446086.1:c.-339T= (CDKL3) XP_024301854.1:n.-339T=
XM_024446093.1:c.227+83T= (CDKL3) XP_024301861.1:n.227+83T=
XM_024446096.1:c.-720T= (CDKL3) XP_024301864.1:n.-720T=
XM_024446097.1:c.-741T= (CDKL3) XP_024301865.1:n.-741T=
XM_024446099.1:c.-439+83T= (CDKL3) XP_024301867.1:n.-439+83T=
XM_024446100.1:c.-541T= (CDKL3) XP_024301868.1:n.-541T=
XM_024446101.1:c.-331T= (CDKL3) XP_024301869.1:n.-331T=
XM_024446103.1:c.-541T= (CDKL3) XP_024301871.1:n.-541T=