MIR4764 microRNA 4764

Information
Symbol
MIR4764
Type
ncRNA
Description
microRNA 4764
Entrez Gene ID
100616295
Genome
hg19
Position
chr22:33,832,568-33,832,655
Genome
hg38
Position
chr22:33,436,582-33,436,669
HGNC
HGNC:41714 HGNC
Ensembl
ENSG00000266012 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:41714 HGNC
Ensembl ENSG00000266012 Ensembl
miRBase MI0017405
AllianceGenome HGNC:41714
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000580680.1 hg38 chr22 33,436,582 33,436,669 88
ENST00000580680.1 hg19 chr22 33,832,568 33,832,655 88
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