APP-DT APP divergent transcript

Information
Symbol
APP-DT
Type
ncRNA
Description
APP divergent transcript
Entrez Gene ID
118568803
Genome
hg19
Position
chr21:27,543,218-27,555,121
Genome
hg38
Position
chr21:26,170,900-26,182,802
HGNC
HGNC:55075 HGNC
Ensembl
ENSG00000273492 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:55075 HGNC
Ensembl ENSG00000273492 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000609365.2 hg38 chr21 26,170,881 26,217,368 46,488
ENST00000664668.1 hg38 chr21 26,170,900 26,182,802 11,903
ENST00000609365.2 hg19 chr21 27,543,199 27,589,687 46,489
ENST00000664668.1 hg19 chr21 27,543,218 27,555,121 11,904
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