MIR4655 microRNA 4655

Information
Symbol
MIR4655
Type
ncRNA
Description
microRNA 4655
Entrez Gene ID
100616160
Genome
hg19
Position
chr7:1,883,816-1,883,889
Genome
hg38
Position
chr7:1,844,180-1,844,253
HGNC
HGNC:41754 HGNC
Ensembl
ENSG00000265089 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
HGNC HGNC:41754 HGNC
Ensembl ENSG00000265089 Ensembl
miRBase MI0017283
AllianceGenome HGNC:41754
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000580817.1 hg38 chr7 1,844,180 1,844,253 74
ENST00000580817.1 hg19 chr7 1,883,816 1,883,889 74
Genome browser