HCG18 HLA complex group 18
Information
- Symbol
- HCG18
- Type
- ncRNA
- Description
- HLA complex group 18
- Entrez Gene ID
- 414777
- Genome
- hg19
- Position
- chr6:30,254,480-30,294,863
- Genome
- hg38
- Position
- chr6:30,286,703-30,327,086
- HGNC
- HGNC:31337 HGNC
- Ensembl
- ENSG00000231074 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
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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000687430.1 | hg38 | chr6 | 30,288,243 | 30,326,362 | 38,120 |
| ENST00000654996.1 | hg38 | chr6 | 30,286,747 | 30,326,701 | 39,955 |
| ENST00000653541.1 | hg38 | chr6 | 30,286,728 | 30,326,866 | 40,139 |
| ENST00000654915.1 | hg38 | chr6 | 30,286,806 | 30,326,393 | 39,588 |
| ENST00000659132.1 | hg38 | chr6 | 30,286,703 | 30,327,086 | 40,384 |
| ENST00000602698.7 | hg38 | chr6 | 30,291,006 | 30,326,825 | 35,820 |
| ENST00000657247.1 | hg38 | chr6 | 30,286,747 | 30,326,868 | 40,122 |
| ENST00000653541.1 | hg19 | chr6 | 30,254,505 | 30,294,643 | 40,139 |
| ENST00000654996.1 | hg19 | chr6 | 30,254,524 | 30,294,478 | 39,955 |
| ENST00000654915.1 | hg19 | chr6 | 30,254,583 | 30,294,170 | 39,588 |
| ENST00000602698.7 | hg19 | chr6 | 30,258,783 | 30,294,602 | 35,820 |
| ENST00000659132.1 | hg19 | chr6 | 30,254,480 | 30,294,863 | 40,384 |
| ENST00000657247.1 | hg19 | chr6 | 30,254,524 | 30,294,645 | 40,122 |
| ENST00000687430.1 | hg19 | chr6 | 30,256,020 | 30,294,139 | 38,120 |
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