CCNB2 cyclin B2

Information
Symbol
CCNB2
Type
protein-coding
Description
cyclin B2
Entrez Gene ID
9133
Genome
hg19
Position
chr15:59,397,345-59,417,244
Genome
hg38
Position
chr15:59,105,146-59,125,045
MIM
602755 OMIM
HGNC
HGNC:1580 HGNC
Ensembl
ENSG00000157456 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 8
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
54
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 HsT17299
MIM 602755 OMIM
HGNC HGNC:1580 HGNC
Ensembl ENSG00000157456 Ensembl
AllianceGenome HGNC:1580
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000621385.1 hg38 chr15 59,105,269 59,125,044 19,776
ENST00000559622.5 hg38 chr15 59,105,157 59,125,016 19,860
ENST00000288207.7 hg38 chr15 59,105,146 59,125,045 19,900
ENST00000288207.7 hg19 chr15 59,397,345 59,417,244 19,900
ENST00000559622.5 hg19 chr15 59,397,356 59,417,215 19,860
ENST00000621385.1 hg19 chr15 59,397,468 59,417,243 19,776
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