Canonical Allele Identifier: CA361462082

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371632T>G , CM000667.2:g.134371632T>G GRCh38
NC_000005.9:g.133707323T>G , CM000667.1:g.133707323T>G GRCh37
NC_000005.8:g.133735222T>G NCBI36
NG_042179.2:g.4416A>C
NG_046936.1:g.5457T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000507277.2:c.37T>G (UBE2B) ENSP00000425137.2:p.Phe13Val
ENST00000265339.7:c.37T>G (UBE2B) MANE Select ENSP00000265339.2:p.Phe13Val
ENST00000265339.6:c.37T>G (UBE2B) ENSP00000265339.2:p.Phe13Val
ENST00000504431.1:n.27T>G (UBE2B)
ENST00000506787.5:c.34T>G (UBE2B) ENSP00000426364.1:p.Phe12Val
ENST00000507277.1:c.29T>G (UBE2B)
ENST00000510021.5:c.37T>G (UBE2B) ENSP00000425237.1:p.Phe13Val
ENST00000511807.1:n.131T>G (UBE2B)
NM_003337.3:c.37T>G (UBE2B) NP_003328.1:p.Phe13Val
XM_024446093.1:c.-8A>C (CDKL3) XP_024301861.1:n.-8A>C
NM_003337.4:c.37T>G (UBE2B) MANE Select NP_003328.1:p.Phe13Val