Canonical Allele Identifier: CA1584037126

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371673C= , CM000667.2:g.134371673C= GRCh38
NC_000005.9:g.133707364C= , CM000667.1:g.133707364C= GRCh37
NC_000005.8:g.133735263C= NCBI36
NG_042179.2:g.4375G=
NG_046936.1:g.5498C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507277.2:c.44+34C= (UBE2B) ENSP00000425137.2:n.44+34C=
ENST00000265339.7:c.44+34C= (UBE2B) MANE Select ENSP00000265339.2:n.44+34C=
ENST00000265339.6:c.44+34C= (UBE2B) ENSP00000265339.2:n.44+34C=
ENST00000504431.1:n.34+34C= (UBE2B)
ENST00000506787.5:c.41+34C= (UBE2B) ENSP00000426364.1:n.41+34C=
ENST00000507277.1:c.36+34C= (UBE2B)
ENST00000510021.5:c.44+34C= (UBE2B) ENSP00000425237.1:n.44+34C=
ENST00000511807.1:n.138+34C= (UBE2B)
NM_003337.3:c.44+34C= (UBE2B) NP_003328.1:n.44+34C=
XM_024446093.1:c.-49G= (CDKL3) XP_024301861.1:n.-49G=
NM_003337.4:c.44+34C= (UBE2B) MANE Select NP_003328.1:n.44+34C=