ASF1B anti-silencing function 1B histone chaperone
Information
- Symbol
- ASF1B
- Type
- protein-coding
- Description
- anti-silencing function 1B histone chaperone
- Entrez Gene ID
- 55723
- Genome
- hg19
- Position
- chr19:14,230,324-14,247,401
- Genome
- hg38
- Position
- chr19:14,119,512-14,136,589
- MIM
- 609190 OMIM
- HGNC
- HGNC:20996 HGNC
- Ensembl
- ENSG00000105011 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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32 |
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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 |
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CIA-II |
MIM | 609190 OMIM |
HGNC | HGNC:20996 HGNC |
Ensembl | ENSG00000105011 Ensembl |
AllianceGenome | HGNC:20996 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000474890.1 | hg38 | chr19 | 14,121,287 | 14,136,574 | 15,288 |
ENST00000263382.8 | hg38 | chr19 | 14,119,512 | 14,136,589 | 17,078 |
ENST00000592798.5 | hg38 | chr19 | 14,120,219 | 14,136,553 | 16,335 |
ENST00000263382.8 | hg19 | chr19 | 14,230,324 | 14,247,401 | 17,078 |
ENST00000592798.5 | hg19 | chr19 | 14,231,031 | 14,247,365 | 16,335 |
ENST00000474890.1 | hg19 | chr19 | 14,232,099 | 14,247,386 | 15,288 |
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