Canonical Allele Identifier: CA1584037095

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371618G= , CM000667.2:g.134371618G= GRCh38
NC_000005.9:g.133707309G= , CM000667.1:g.133707309G= GRCh37
NC_000005.8:g.133735208G= NCBI36
NG_042179.2:g.4430C=
NG_046936.1:g.5443G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507277.2:c.23G= (UBE2B) ENSP00000425137.2:p.Arg8=
ENST00000265339.7:c.23G= (UBE2B) MANE Select ENSP00000265339.2:p.Arg8=
ENST00000265339.6:c.23G= (UBE2B) ENSP00000265339.2:p.Arg8=
ENST00000504431.1:n.13G= (UBE2B)
ENST00000506787.5:c.20G= (UBE2B) ENSP00000426364.1:p.Arg7=
ENST00000507277.1:c.15G= (UBE2B)
ENST00000510021.5:c.23G= (UBE2B) ENSP00000425237.1:p.Arg8=
ENST00000511807.1:n.117G= (UBE2B)
NM_003337.3:c.23G= (UBE2B) NP_003328.1:p.Arg8=
XM_024446093.1:c.7C= (CDKL3) XP_024301861.1:p.Leu3=
NM_003337.4:c.23G= (UBE2B) MANE Select NP_003328.1:p.Arg8=