MIR5692B microRNA 5692b

Information
Symbol
MIR5692B
Type
ncRNA
Description
microRNA 5692b
Entrez Gene ID
100847013
Genome
hg19
Position
chr21:44,371,038-44,371,124
Genome
hg38
Position
chr21:42,950,928-42,951,014
HGNC
HGNC:43535 HGNC
Ensembl
ENSG00000264580 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:43535 HGNC
Ensembl ENSG00000264580 Ensembl
miRBase MI0019311
AllianceGenome HGNC:43535
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000579137.1 hg38 chr21 42,950,928 42,951,014 87
ENST00000579137.1 hg19 chr21 44,371,038 44,371,124 87
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