MIR4728 microRNA 4728

Information
Symbol
MIR4728
Type
ncRNA
Description
microRNA 4728
Entrez Gene ID
100616132
Genome
hg19
Position
chr17:37,882,748-37,882,814
Genome
hg38
Position
chr17:39,726,495-39,726,561
HGNC
HGNC:41632 HGNC
Ensembl
ENSG00000265178 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 5 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
HGNC HGNC:41632 HGNC
Ensembl ENSG00000265178 Ensembl
miRBase MI0017365
AllianceGenome HGNC:41632
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000580969.1 hg38 chr17 39,726,495 39,726,561 67
ENST00000580969.1 hg19 chr17 37,882,748 37,882,814 67
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