HCG27 HLA complex group 27
Information
- Symbol
- HCG27
- Type
- ncRNA
- Description
- HLA complex group 27
- Entrez Gene ID
- 253018
- Genome
- hg19
- Position
- chr6:31,165,537-31,171,745
- Genome
- hg38
- Position
- chr6:31,197,760-31,203,968
- HGNC
- HGNC:27366 HGNC
- Ensembl
- ENSG00000206344 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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0 |
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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
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| 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 | |||||||||||
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MGeND data only
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| 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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| 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 | bCX101P6.9 |
| SYNONYM | bPG299F13.9 |
| SYNONYM | bQB115I13.2 |
| HGNC | HGNC:27366 HGNC |
| Ensembl | ENSG00000206344 Ensembl |
| AllianceGenome | HGNC:27366 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000383331.4 | hg38 | chr6 | 31,197,760 | 31,203,968 | 6,209 |
| ENST00000383331.4 | hg19 | chr6 | 31,165,537 | 31,171,745 | 6,209 |
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