Canonical Allele Identifier: CA1584036776

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371312A= , CM000667.2:g.134371312A= GRCh38
NC_000005.9:g.133707003A= , CM000667.1:g.133707003A= GRCh37
NC_000005.8:g.133734902A= NCBI36
NG_042179.2:g.4736T=
NG_046936.1:g.5137A=

Transcript Alleles

HGVS Amino-acid change
ENST00000507277.2:c.-284A= (UBE2B) ENSP00000425137.2:n.-284A=
ENST00000265339.6:c.-284A= (UBE2B) ENSP00000265339.2:n.-284A=
NM_003337.3:c.-284A= (UBE2B) NP_003328.1:n.-284A=
XM_011543441.1:c.-224+86T= (CDKL3) XP_011541743.1:n.-224+86T=
XM_017009544.2:c.-946T= (CDKL3) XP_016865033.1:n.-946T=
XM_017009545.2:c.-751T= (CDKL3) XP_016865034.1:n.-751T=
XM_024446086.1:c.-336T= (CDKL3) XP_024301854.1:n.-336T=
XM_024446093.1:c.227+86T= (CDKL3) XP_024301861.1:n.227+86T=
XM_024446096.1:c.-717T= (CDKL3) XP_024301864.1:n.-717T=
XM_024446097.1:c.-738T= (CDKL3) XP_024301865.1:n.-738T=
XM_024446099.1:c.-439+86T= (CDKL3) XP_024301867.1:n.-439+86T=
XM_024446100.1:c.-538T= (CDKL3) XP_024301868.1:n.-538T=
XM_024446101.1:c.-328T= (CDKL3) XP_024301869.1:n.-328T=
XM_024446103.1:c.-538T= (CDKL3) XP_024301871.1:n.-538T=