LINC01479 long intergenic non-protein coding RNA 1479
Information
- Symbol
- LINC01479
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1479
- Entrez Gene ID
- 101927922
- Genome
- hg19
- Position
- chr12:68,323,015-68,326,728
- Genome
- hg38
- Position
- chr12:67,929,235-67,932,948
- HGNC
- HGNC:51123 HGNC
- Ensembl
- ENSG00000255772 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
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| 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
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| 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
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| Category | : |
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | HRAT39 |
| HGNC | HGNC:51123 HGNC |
| Ensembl | ENSG00000255772 Ensembl |
| AllianceGenome | HGNC:51123 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000546170.1 | hg38 | chr12 | 67,929,263 | 67,970,017 | 40,755 |
| ENST00000545520.5 | hg38 | chr12 | 67,929,235 | 67,932,948 | 3,714 |
| ENST00000545520.5 | hg19 | chr12 | 68,323,015 | 68,326,728 | 3,714 |
| ENST00000546170.1 | hg19 | chr12 | 68,323,043 | 68,363,797 | 40,755 |
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