LINC00486 long intergenic non-protein coding RNA 486

Information
Symbol
LINC00486
Type
ncRNA
Description
long intergenic non-protein coding RNA 486
Entrez Gene ID
285045
Genome
hg19
Position
chr2:33,050,489-33,067,632
Genome
hg38
Position
chr2:32,825,422-32,842,565
HGNC
HGNC:42946 HGNC
Ensembl
ENSG00000230876 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:42946 HGNC
Ensembl ENSG00000230876 Ensembl
AllianceGenome HGNC:42946
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000414054.5 hg38 chr2 32,825,443 32,926,693 101,251
ENST00000424364.6 hg38 chr2 32,841,014 32,902,123 61,110
ENST00000663772.1 hg38 chr2 32,825,422 32,842,565 17,144
ENST00000657199.1 hg38 chr2 32,825,440 32,842,622 17,183
ENST00000648808.2 hg38 chr2 32,825,359 32,842,597 17,239
ENST00000648808.2 hg19 chr2 33,050,426 33,067,664 17,239
ENST00000663772.1 hg19 chr2 33,050,489 33,067,632 17,144
ENST00000657199.1 hg19 chr2 33,050,507 33,067,689 17,183
ENST00000414054.5 hg19 chr2 33,050,510 33,151,760 101,251
ENST00000424364.6 hg19 chr2 33,066,081 33,127,190 61,110
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