MIR892C microRNA 892c

Information
Symbol
MIR892C
Type
ncRNA
Description
microRNA 892c
Entrez Gene ID
102466721
Genome
hg19
Position
chrX:145,074,271-145,074,343
Genome
hg38
Position
chrX:145,992,750-145,992,826
HGNC
HGNC:50194 HGNC
Ensembl
ENSG00000252219 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 hsa-mir-892c
HGNC HGNC:50194 HGNC
Ensembl ENSG00000252219 Ensembl
miRBase MI0022560
AllianceGenome HGNC:50194
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000516410.2 hg38 chrX 145,992,750 145,992,826 77
ENST00000516410.1 hg19 chrX 145,074,271 145,074,343 73
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