LINC02932 long intergenic non-protein coding RNA 2932
Information
- Symbol
- LINC02932
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2932
- Entrez Gene ID
- 105375392
- Genome
- hg19
- Position
- chr7:91,084,871-91,143,862
- Genome
- hg38
- Position
- chr7:91,455,556-91,514,547
- HGNC
- HGNC:55875 HGNC
- Ensembl
- ENSG00000243144 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000667320.1 | hg38 | chr7 | 91,455,593 | 91,515,427 | 59,835 |
ENST00000449361.5 | hg38 | chr7 | 91,311,368 | 91,335,741 | 24,374 |
ENST00000664526.1 | hg38 | chr7 | 91,455,556 | 91,514,547 | 58,992 |
ENST00000449361.5 | hg19 | chr7 | 90,940,683 | 90,965,056 | 24,374 |
ENST00000664526.1 | hg19 | chr7 | 91,084,871 | 91,143,862 | 58,992 |
ENST00000667320.1 | hg19 | chr7 | 91,084,908 | 91,144,742 | 59,835 |
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