Canonical Allele Identifier: CA361462098

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371635A>T , CM000667.2:g.134371635A>T GRCh38
NC_000005.9:g.133707326A>T , CM000667.1:g.133707326A>T GRCh37
NC_000005.8:g.133735225A>T NCBI36
NG_042179.2:g.4413T>A
NG_046936.1:g.5460A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000507277.2:c.40A>T (UBE2B) ENSP00000425137.2:p.Lys14Ter
ENST00000265339.7:c.40A>T (UBE2B) MANE Select ENSP00000265339.2:p.Lys14Ter
ENST00000265339.6:c.40A>T (UBE2B) ENSP00000265339.2:p.Lys14Ter
ENST00000504431.1:n.30A>T (UBE2B)
ENST00000506787.5:c.37A>T (UBE2B) ENSP00000426364.1:p.Lys13Ter
ENST00000507277.1:c.32A>T (UBE2B)
ENST00000510021.5:c.40A>T (UBE2B) ENSP00000425237.1:p.Lys14Ter
ENST00000511807.1:n.134A>T (UBE2B)
NM_003337.3:c.40A>T (UBE2B) NP_003328.1:p.Lys14Ter
XM_024446093.1:c.-11T>A (CDKL3) XP_024301861.1:n.-11T>A
NM_003337.4:c.40A>T (UBE2B) MANE Select NP_003328.1:p.Lys14Ter