MIR4487 microRNA 4487

Information
Symbol
MIR4487
Type
ncRNA
Description
microRNA 4487
Entrez Gene ID
100616222
Genome
hg19
Position
chr11:47,422,521-47,422,593
Genome
hg38
Position
chr11:47,400,970-47,401,042
HGNC
HGNC:41851 HGNC
Ensembl
ENSG00000264583 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
SYNONYM mir-4487
HGNC HGNC:41851 HGNC
Ensembl ENSG00000264583 Ensembl
miRBase MI0016848
AllianceGenome HGNC:41851
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000582237.1 hg38 chr11 47,400,970 47,401,042 73
ENST00000582237.1 hg19 chr11 47,422,521 47,422,593 73
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