Canonical Allele Identifier: CA12011530
Gene: UBE2D2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs261532

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139569777G>T , CM000667.2:g.139569777G>T GRCh38
NC_000005.8:g.138929546G>T NCBI36
NC_000005.9:g.138949362G>T , CM000667.1:g.138949362G>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000398733.7:c.24+7962G>T ENSP00000381717.3:p.=
ENST00000398734.8:c.24+7962G>T ENSP00000381718.4:p.=
ENST00000505007.5:c.-64+7370G>T ENSP00000426523.1:p.=
ENST00000505548.5:c.-64+7370G>T ENSP00000424941.1:p.=
ENST00000510470.1:n.92+7962G>T
ENST00000511725.5:c.-63-30595G>T ENSP00000429613.1:p.=
NM_003339.2:c.24+7962G>T VV NP_003330.1:p.=
NM_181838.1:c.-64+7370G>T VV NP_862821.1:p.=
XM_017009820.1:c.-96+7146G>T XP_016865309.1:p.=