IGHV4-30-2 immunoglobulin heavy variable 4-30-2
Information
- Symbol
- IGHV4-30-2
- Type
- other
- Description
- immunoglobulin heavy variable 4-30-2
- Entrez Gene ID
- 28398
- Genome
- hg19
- Position
- chr14:106,805,209-106,805,716
- Genome
- hg38
- Position
- chr14:106,349,283-106,349,792
- HGNC
- HGNC:5647 HGNC
- Ensembl
- ENSG00000231475 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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0 |
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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
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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 | |||||||||||
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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 | IGHV4-3 |
| SYNONYM | IGHV4302 |
| HGNC | HGNC:5647 HGNC |
| Ensembl | ENSG00000231475 Ensembl |
| IMGT/GENE-DB | IGHV4-30-2 |
| AllianceGenome | HGNC:5647 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000438142.3 | hg38 | chr14 | 106,349,283 | 106,349,792 | 510 |
| ENST00000438142.2 | hg19 | chr14 | 106,805,209 | 106,805,716 | 508 |
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