CCNG2 cyclin G2

Information
Symbol
CCNG2
Type
protein-coding
Description
cyclin G2
Entrez Gene ID
901
Genome
hg19
Position
chr4:78,078,360-78,091,213
Genome
hg38
Position
chr4:77,157,207-77,170,060
MIM
603203 OMIM
HGNC
HGNC:1593 HGNC
Ensembl
ENSG00000138764 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
34
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 :
Filtering :
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
MIM 603203 OMIM
HGNC HGNC:1593 HGNC
Ensembl ENSG00000138764 Ensembl
AllianceGenome HGNC:1593
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000395640.5 hg38 chr4 77,158,297 77,166,063 7,767
ENST00000316355.10 hg38 chr4 77,157,207 77,170,060 12,854
ENST00000509972.1 hg38 chr4 77,158,426 77,165,010 6,585
ENST00000502280.5 hg38 chr4 77,157,210 77,166,184 8,975
ENST00000316355.10 hg19 chr4 78,078,360 78,091,213 12,854
ENST00000502280.5 hg19 chr4 78,078,363 78,087,337 8,975
ENST00000395640.5 hg19 chr4 78,079,450 78,087,216 7,767
ENST00000509972.1 hg19 chr4 78,079,579 78,086,163 6,585
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