LOC101927708 uncharacterized LOC101927708

Information
Symbol
LOC101927708
Type
ncRNA
Description
uncharacterized LOC101927708
Entrez Gene ID
101927708
Genome
hg19
Position
chr11:3,502,750-3,602,441
Genome
hg38
Position
chr11:3,481,520-3,581,211
Ensembl
ENSG00000255367 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
Ensembl ENSG00000255367 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000710269.1 hg38 chr11 3,475,778 3,580,966 105,189
ENST00000527970.1 hg38 chr11 3,481,520 3,581,211 99,692
ENST00000526533.1 hg38 chr11 3,507,980 3,571,987 64,008
ENST00000710269.1 hg19 chr11 3,497,008 3,602,196 105,189
ENST00000527970.1 hg19 chr11 3,502,750 3,602,441 99,692
ENST00000526533.1 hg19 chr11 3,529,210 3,593,217 64,008
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