CSNK1G2-AS1 CSNK1G2 antisense RNA 1
Information
- Symbol
- CSNK1G2-AS1
- Type
- ncRNA
- Description
- CSNK1G2 antisense RNA 1
- Entrez Gene ID
- 255193
- Genome
- hg19
- Position
- chr19:1,952,588-1,954,585
- Genome
- hg38
- Position
- chr19:1,952,589-1,954,586
- HGNC
- HGNC:28604 HGNC
- Ensembl
- ENSG00000180846 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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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 |
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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 | |||
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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 |
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SYNONYM | C19orf34 |
HGNC | HGNC:28604 HGNC |
Ensembl | ENSG00000180846 Ensembl |
AllianceGenome | HGNC:28604 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000586395.2 | hg38 | chr19 | 1,952,589 | 1,954,586 | 1,998 |
ENST00000586395.2 | hg19 | chr19 | 1,952,588 | 1,954,585 | 1,998 |
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