HLA-F major histocompatibility complex, class I, F
Information
- Symbol
- HLA-F
- Type
- protein-coding
- Description
- major histocompatibility complex, class I, F
- Entrez Gene ID
- 3134
- Genome
- hg19
- Position
- chr6:29,691,211-29,695,073
- Genome
- hg38
- Position
- chr6:29,723,434-29,727,296
- MIM
- 143110 OMIM
- HGNC
- HGNC:4963 HGNC
- Ensembl
- ENSG00000204642 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 24 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
4 |
 |
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
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 | CDA12 |
| SYNONYM | HLA-5.4 |
| SYNONYM | HLA-CDA12 |
| SYNONYM | HLAF |
| MIM | 143110 OMIM |
| HGNC | HGNC:4963 HGNC |
| Ensembl | ENSG00000204642 Ensembl |
| AllianceGenome | HGNC:4963 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000259951.12 | hg38 | chr6 | 29,723,434 | 29,727,296 | 3,863 |
| ENST00000334668.8 | hg38 | chr6 | 29,723,340 | 29,726,525 | 3,186 |
| ENST00000434407.6 | hg38 | chr6 | 29,723,464 | 29,726,526 | 3,063 |
| ENST00000376861.5 | hg38 | chr6 | 29,722,775 | 29,726,526 | 3,752 |
| ENST00000376861.5 | hg19 | chr6 | 29,690,552 | 29,694,303 | 3,752 |
| ENST00000334668.8 | hg19 | chr6 | 29,691,117 | 29,694,302 | 3,186 |
| ENST00000259951.12 | hg19 | chr6 | 29,691,211 | 29,695,073 | 3,863 |
| ENST00000434407.6 | hg19 | chr6 | 29,691,241 | 29,694,303 | 3,063 |
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