HLA-G major histocompatibility complex, class I, G
Information
- Symbol
- HLA-G
- Type
- protein-coding
- Description
- major histocompatibility complex, class I, G
- Entrez Gene ID
- 3135
- Genome
- hg19
- Position
- chr6:29,794,744-29,798,902
- Genome
- hg38
- Position
- chr6:29,826,967-29,831,125
- MIM
- 142871 OMIM
- HGNC
- HGNC:4964 HGNC
- Ensembl
- ENSG00000204632 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 6 |
| Likely risk allele | 0 | 2 |
| not provided | 40 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
2 |
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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| Category | : |
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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
|
| 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 | MHC-G |
| MIM | 142871 OMIM |
| HGNC | HGNC:4964 HGNC |
| Ensembl | ENSG00000204632 Ensembl |
| AllianceGenome | HGNC:4964 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000376815.3 | hg38 | chr6 | 29,827,845 | 29,831,125 | 3,281 |
| ENST00000376818.7 | hg38 | chr6 | 29,827,845 | 29,831,125 | 3,281 |
| ENST00000376828.6 | hg38 | chr6 | 29,826,967 | 29,831,125 | 4,159 |
| ENST00000360323.11 | hg38 | chr6 | 29,827,825 | 29,831,021 | 3,197 |
| ENST00000376828.6 | hg19 | chr6 | 29,794,744 | 29,798,902 | 4,159 |
| ENST00000360323.11 | hg19 | chr6 | 29,795,602 | 29,798,798 | 3,197 |
| ENST00000376815.3 | hg19 | chr6 | 29,795,622 | 29,798,902 | 3,281 |
| ENST00000376818.7 | hg19 | chr6 | 29,795,622 | 29,798,902 | 3,281 |
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