LINC00454 long intergenic non-protein coding RNA 454
Information
- Symbol
- LINC00454
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 454
- Entrez Gene ID
- 100874178
- Genome
- hg19
- Position
- chr13:114,581,603-114,584,349
- Genome
- hg38
- Position
- chr13:113,878,630-113,881,376
- HGNC
- HGNC:42802 HGNC
- Ensembl
- ENSG00000226921 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 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000661456.1 | hg38 | chr13 | 113,878,628 | 113,883,649 | 5,022 |
ENST00000671045.1 | hg38 | chr13 | 113,878,630 | 113,881,376 | 2,747 |
ENST00000430978.7 | hg38 | chr13 | 113,878,489 | 113,883,557 | 5,069 |
ENST00000430978.7 | hg19 | chr13 | 114,581,462 | 114,586,530 | 5,069 |
ENST00000661456.1 | hg19 | chr13 | 114,581,601 | 114,586,622 | 5,022 |
ENST00000671045.1 | hg19 | chr13 | 114,581,603 | 114,584,349 | 2,747 |
Genome browser