Canonical Allele Identifier: CA2768485756

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371220G>C , CM000667.2:g.134371220G>C GRCh38
NC_000005.9:g.133706911G>C , CM000667.1:g.133706911G>C GRCh37
NC_000005.8:g.133734810G>C NCBI36
NG_042179.2:g.4828C>G
NG_046936.1:g.5045G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000507277.2:c.-376G>C (UBE2B) ENSP00000425137.2:n.-376G>C
ENST00000265339.6:c.-376G>C (UBE2B) ENSP00000265339.2:n.-376G>C
NM_003337.3:c.-376G>C (UBE2B) NP_003328.1:n.-376G>C
XM_011543441.1:c.-224+178C>G (CDKL3) XP_011541743.1:n.-224+178C>G
XM_017009544.2:c.-854C>G (CDKL3) XP_016865033.1:n.-854C>G
XM_017009545.2:c.-659C>G (CDKL3) XP_016865034.1:n.-659C>G
XM_024446086.1:c.-244C>G (CDKL3) XP_024301854.1:n.-244C>G
XM_024446093.1:c.227+178C>G (CDKL3) XP_024301861.1:n.227+178C>G
XM_024446096.1:c.-625C>G (CDKL3) XP_024301864.1:n.-625C>G
XM_024446097.1:c.-646C>G (CDKL3) XP_024301865.1:n.-646C>G
XM_024446099.1:c.-439+178C>G (CDKL3) XP_024301867.1:n.-439+178C>G
XM_024446100.1:c.-446C>G (CDKL3) XP_024301868.1:n.-446C>G
XM_024446101.1:c.-236C>G (CDKL3) XP_024301869.1:n.-236C>G
XM_024446103.1:c.-446C>G (CDKL3) XP_024301871.1:n.-446C>G