LINC02386 long intergenic non-protein coding RNA 2386

Information
Symbol
LINC02386
Type
ncRNA
Description
long intergenic non-protein coding RNA 2386
Entrez Gene ID
105369717
Genome
hg19
Position
chr12:30,383,712-30,449,640
Genome
hg38
Position
chr12:30,230,779-30,296,707
HGNC
HGNC:53312 HGNC
Ensembl
ENSG00000257756 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:53312 HGNC
Ensembl ENSG00000257756 Ensembl
AllianceGenome HGNC:53312
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000663022.1 hg38 chr12 30,230,779 30,296,707 65,929
ENST00000655472.1 hg38 chr12 30,230,780 30,296,703 65,924
ENST00000551202.1 hg38 chr12 30,230,785 30,296,664 65,880
ENST00000551287.1 hg38 chr12 30,294,447 30,296,707 2,261
ENST00000666420.1 hg38 chr12 30,230,779 30,296,703 65,925
ENST00000666420.1 hg19 chr12 30,383,712 30,449,636 65,925
ENST00000663022.1 hg19 chr12 30,383,712 30,449,640 65,929
ENST00000655472.1 hg19 chr12 30,383,713 30,449,636 65,924
ENST00000551202.1 hg19 chr12 30,383,718 30,449,597 65,880
ENST00000551287.1 hg19 chr12 30,447,380 30,449,640 2,261
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