MIR891B microRNA 891b

Information
Symbol
MIR891B
Type
ncRNA
Description
microRNA 891b
Entrez Gene ID
100126304
Genome
hg19
Position
chrX:145,082,571-145,082,649
Genome
hg38
Position
chrX:146,001,053-146,001,131
HGNC
HGNC:33645 HGNC
Ensembl
ENSG00000216064 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 MIRN891B
HGNC HGNC:33645 HGNC
Ensembl ENSG00000216064 Ensembl
miRBase MI0005534
AllianceGenome HGNC:33645
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000401245.1 hg38 chrX 146,001,053 146,001,131 79
ENST00000401245.1 hg19 chrX 145,082,571 145,082,649 79
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