MIR892B microRNA 892b

Information
Symbol
MIR892B
Type
ncRNA
Description
microRNA 892b
Entrez Gene ID
100126307
Genome
hg19
Position
chrX:145,078,716-145,078,792
Genome
hg38
Position
chrX:145,997,198-145,997,274
HGNC
HGNC:33649 HGNC
Ensembl
ENSG00000216098 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 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
SYNONYM MIRN892B
HGNC HGNC:33649 HGNC
Ensembl ENSG00000216098 Ensembl
miRBase MI0005538
AllianceGenome HGNC:33649
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000401279.1 hg38 chrX 145,997,198 145,997,274 77
ENST00000401279.1 hg19 chrX 145,078,716 145,078,792 77
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