SRRM2-AS1 SRRM2 antisense RNA 1

Information
Symbol
SRRM2-AS1
Type
ncRNA
Description
SRRM2 antisense RNA 1
Entrez Gene ID
100128788
Genome
hg19
Position
chr16:2,787,092-2,790,805
Genome
hg38
Position
chr16:2,737,091-2,740,804
HGNC
HGNC:44162 HGNC
Ensembl
ENSG00000205913 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:44162 HGNC
Ensembl ENSG00000205913 Ensembl
AllianceGenome HGNC:44162
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000571305.5 hg38 chr16 2,737,103 2,744,797 7,695
ENST00000573802.1 hg38 chr16 2,737,103 2,752,600 15,498
ENST00000577055.5 hg38 chr16 2,737,076 2,750,810 13,735
ENST00000382313.2 hg38 chr16 2,737,091 2,740,804 3,714
ENST00000667280.1 hg38 chr16 2,737,086 2,752,593 15,508
ENST00000577055.5 hg19 chr16 2,787,077 2,800,811 13,735
ENST00000667280.1 hg19 chr16 2,787,087 2,802,594 15,508
ENST00000382313.2 hg19 chr16 2,787,092 2,790,805 3,714
ENST00000571305.5 hg19 chr16 2,787,104 2,794,798 7,695
ENST00000573802.1 hg19 chr16 2,787,104 2,802,601 15,498
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