RNF213-AS1 RNF213 antisense RNA 1

Information
Symbol
RNF213-AS1
Type
ncRNA
Description
RNF213 antisense RNA 1
Entrez Gene ID
100294362
Genome
hg19
Position
chr17:78,325,628-78,388,918
Genome
hg38
Position
chr17:80,351,828-80,415,118
HGNC
HGNC:54402 HGNC
Ensembl
ENSG00000263069 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:54402 HGNC
Ensembl ENSG00000263069 Ensembl
AllianceGenome HGNC:54402
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000667202.1 hg38 chr17 80,359,608 80,415,117 55,510
ENST00000575034.5 hg38 chr17 80,351,828 80,415,118 63,291
ENST00000575034.5 hg19 chr17 78,325,628 78,388,918 63,291
ENST00000667202.1 hg19 chr17 78,333,408 78,388,917 55,510
Genome browser