Canonical Allele Identifier: CA446650579

Linked Data

MyVariant Identifiers: chr5:g.133707313C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371622C>G , CM000667.2:g.134371622C>G GRCh38
NC_000005.9:g.133707313C>G , CM000667.1:g.133707313C>G GRCh37
NC_000005.8:g.133735212C>G NCBI36
NG_042179.2:g.4426G>C
NG_046936.1:g.5447C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000507277.2:c.27C>G (UBE2B) ENSP00000425137.2:p.Leu9=
ENST00000265339.7:c.27C>G (UBE2B) MANE Select ENSP00000265339.2:p.Leu9=
ENST00000265339.6:c.27C>G (UBE2B) ENSP00000265339.2:p.Leu9=
ENST00000504431.1:n.17C>G (UBE2B)
ENST00000506787.5:c.24C>G (UBE2B) ENSP00000426364.1:p.Leu8=
ENST00000507277.1:c.19C>G (UBE2B)
ENST00000510021.5:c.27C>G (UBE2B) ENSP00000425237.1:p.Leu9=
ENST00000511807.1:n.121C>G (UBE2B)
NM_003337.3:c.27C>G (UBE2B) NP_003328.1:p.Leu9=
XM_024446093.1:c.3G>C (CDKL3) XP_024301861.1:p.Met1Ile
NM_003337.4:c.27C>G (UBE2B) MANE Select NP_003328.1:p.Leu9=