Canonical Allele Identifier: CA2710231356
Gene: UBE2D2 HGNC NCBI

Linked Data

dbSNP Id: rs2126653851

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139569775C>T , CM000667.2:g.139569775C>T GRCh38
NC_000005.9:g.138949360C>T , CM000667.1:g.138949360C>T GRCh37
NC_000005.8:g.138929544C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000698321.1:c.-162+7368C>T ENSP00000513666.1:n.-162+7368C>T
ENST00000398733.8:c.24+7960C>T MANE Select ENSP00000381717.3:n.24+7960C>T
ENST00000398733.7:c.24+7960C>T ENSP00000381717.3:n.24+7960C>T
ENST00000398734.8:c.24+7960C>T ENSP00000381718.4:n.24+7960C>T
ENST00000505007.5:c.-64+7368C>T ENSP00000426523.1:n.-64+7368C>T
ENST00000505548.5:c.-64+7368C>T ENSP00000424941.1:n.-64+7368C>T
ENST00000510470.1:n.92+7960C>T
ENST00000511725.5:c.-63-30597C>T ENSP00000429613.1:n.-63-30597C>T
NM_003339.2:c.24+7960C>T NP_003330.1:n.24+7960C>T
NM_181838.1:c.-64+7368C>T NP_862821.1:n.-64+7368C>T
XM_017009820.1:c.-96+7144C>T XP_016865309.1:n.-96+7144C>T
NM_003339.3:c.24+7960C>T MANE Select NP_003330.1:n.24+7960C>T
NM_181838.2:c.-64+7368C>T NP_862821.1:n.-64+7368C>T