MIR4632 microRNA 4632

Information
Symbol
MIR4632
Type
ncRNA
Description
microRNA 4632
Entrez Gene ID
100616438
Genome
hg19
Position
chr1:12,251,770-12,251,830
Genome
hg38
Position
chr1:12,191,713-12,191,773
HGNC
HGNC:41593 HGNC
Ensembl
ENSG00000263676 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:41593 HGNC
Ensembl ENSG00000263676 Ensembl
miRBase MI0017259
AllianceGenome HGNC:41593
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584158.1 hg38 chr1 12,191,713 12,191,773 61
ENST00000584158.1 hg19 chr1 12,251,770 12,251,830 61
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