ELOB elongin B

Information
Symbol
ELOB
Type
protein-coding
Description
elongin B
Entrez Gene ID
6923
Genome
hg19
Position
chr16:2,821,415-2,827,278
Genome
hg38
Position
chr16:2,771,414-2,777,277
MIM
600787 OMIM
HGNC
HGNC:11619 HGNC
Ensembl
ENSG00000103363 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
36
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM SIII
SYNONYM TCEB2
MIM 600787 OMIM
HGNC HGNC:11619 HGNC
Ensembl ENSG00000103363 Ensembl
AllianceGenome HGNC:11619
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409477.1 hg38 chr16 2,771,415 2,777,195 5,781
ENST00000572954.1 hg38 chr16 2,771,943 2,777,272 5,330
ENST00000262306.11 hg38 chr16 2,771,414 2,777,277 5,864
ENST00000691758.1 hg38 chr16 2,772,020 2,776,908 4,889
ENST00000688784.1 hg38 chr16 2,771,938 2,776,789 4,852
ENST00000693239.1 hg38 chr16 2,772,140 2,777,289 5,150
ENST00000409906.9 hg38 chr16 2,771,414 2,777,280 5,867
ENST00000262306.11 hg19 chr16 2,821,415 2,827,278 5,864
ENST00000409906.9 hg19 chr16 2,821,415 2,827,281 5,867
ENST00000409477.1 hg19 chr16 2,821,416 2,827,196 5,781
ENST00000688784.1 hg19 chr16 2,821,939 2,826,790 4,852
ENST00000572954.1 hg19 chr16 2,821,944 2,827,273 5,330
ENST00000691758.1 hg19 chr16 2,822,021 2,826,909 4,889
ENST00000693239.1 hg19 chr16 2,822,141 2,827,290 5,150
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