LINC00449 long intergenic non-protein coding RNA 449

Information
Symbol
LINC00449
Type
ncRNA
Description
long intergenic non-protein coding RNA 449
Entrez Gene ID
106478991
Genome
hg19
Position
chr13:100,143,729-100,148,992
Genome
hg38
Position
chr13:99,491,475-99,496,738
HGNC
HGNC:42786 HGNC
Ensembl
ENSG00000280734 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:42786 HGNC
Ensembl ENSG00000280734 Ensembl
AllianceGenome HGNC:42786
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000626729.2 hg38 chr13 99,491,475 99,496,738 5,264
ENST00000366259.2 hg38 chr13 99,499,727 99,501,052 1,326
ENST00000715702.1 hg38 chr13 99,496,509 99,501,212 4,704
ENST00000715701.1 hg38 chr13 99,495,135 99,501,242 6,108
ENST00000656995.1 hg38 chr13 99,494,378 99,498,806 4,429
ENST00000630421.2 hg38 chr13 99,486,962 99,496,772 9,811
ENST00000630421.2 hg19 chr13 100,139,216 100,149,026 9,811
ENST00000626729.2 hg19 chr13 100,143,729 100,148,992 5,264
ENST00000656995.1 hg19 chr13 100,146,632 100,151,060 4,429
ENST00000715701.1 hg19 chr13 100,147,389 100,153,496 6,108
ENST00000715702.1 hg19 chr13 100,148,763 100,153,466 4,704
ENST00000366259.2 hg19 chr13 100,151,981 100,153,306 1,326
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