MIR4756 microRNA 4756

Information
Symbol
MIR4756
Type
ncRNA
Description
microRNA 4756
Entrez Gene ID
100616225
Genome
hg19
Position
chr20:52,684,947-52,685,024
Genome
hg38
Position
chr20:54,068,408-54,068,485
HGNC
HGNC:41529 HGNC
Ensembl
ENSG00000265595 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
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
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:41529 HGNC
Ensembl ENSG00000265595 Ensembl
miRBase MI0017397
AllianceGenome HGNC:41529
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577874.1 hg38 chr20 54,068,408 54,068,485 78
ENST00000577874.1 hg19 chr20 52,684,947 52,685,024 78
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