D21S2088E D21S2088E

Information
Symbol
D21S2088E
Type
ncRNA
Description
D21S2088E
Entrez Gene ID
266917
Genome
hg19
Position
chr21:24,725,251-24,757,121
Genome
hg38
Position
chr21:23,352,929-23,384,800
Ensembl
ENSG00000228592 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
Ensembl ENSG00000228592 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000656174.1 hg38 chr21 23,361,735 23,423,778 62,044
ENST00000655729.1 hg38 chr21 23,352,929 23,384,800 31,872
ENST00000654898.1 hg38 chr21 23,361,764 23,384,846 23,083
ENST00000653972.1 hg38 chr21 23,361,738 23,423,358 61,621
ENST00000655729.1 hg19 chr21 24,725,251 24,757,121 31,871
ENST00000656174.1 hg19 chr21 24,734,057 24,796,098 62,042
ENST00000653972.1 hg19 chr21 24,734,060 24,795,678 61,619
ENST00000654898.1 hg19 chr21 24,734,086 24,757,167 23,082
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