ABCF2-H2BK1 ABCF2-H2BK1 readthrough
Information
- Symbol
- ABCF2-H2BK1
- Type
- protein-coding
- Description
- ABCF2-H2BK1 readthrough
- Entrez Gene ID
- 114483834
- Genome
- hg19
- Position
- chr7:150,904,923-150,924,252
- Genome
- hg38
- Position
- chr7:151,207,837-151,227,166
- HGNC
- HGNC:54751 HGNC
- Ensembl
- ENSG00000285292 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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24 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | ABCF2-H2BE1 |
HGNC | HGNC:54751 HGNC |
Ensembl | ENSG00000285292 Ensembl |
AllianceGenome | HGNC:54751 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000222388.6 | hg38 | chr7 | 151,207,837 | 151,227,166 | 19,330 |
ENST00000222388.6 | hg19 | chr7 | 150,904,923 | 150,924,252 | 19,330 |
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