LINC02446 long intergenic non-protein coding RNA 2446

Information
Symbol
LINC02446
Type
ncRNA
Description
long intergenic non-protein coding RNA 2446
Entrez Gene ID
101060038
Genome
hg19
Position
chr12:10,705,961-10,711,395
Genome
hg38
Position
chr12:10,553,362-10,558,796
HGNC
HGNC:53378 HGNC
Ensembl
ENSG00000256039 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:53378 HGNC
Ensembl ENSG00000256039 Ensembl
AllianceGenome HGNC:53378
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000544591.2 hg38 chr12 10,553,362 10,558,796 5,435
ENST00000702593.1 hg38 chr12 10,553,365 10,570,374 17,010
ENST00000702299.1 hg38 chr12 10,553,364 10,572,761 19,398
ENST00000652990.1 hg38 chr12 10,553,362 10,572,688 19,327
ENST00000544591.2 hg19 chr12 10,705,961 10,711,395 5,435
ENST00000652990.1 hg19 chr12 10,705,961 10,725,287 19,327
ENST00000702299.1 hg19 chr12 10,705,963 10,725,360 19,398
ENST00000702593.1 hg19 chr12 10,705,964 10,722,973 17,010
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