NCBP2AS2 NCBP2 antisense 2 (head to head)
Information
- Symbol
- NCBP2AS2
- Type
- protein-coding
- Description
- NCBP2 antisense 2 (head to head)
- Entrez Gene ID
- 152217
- Genome
- hg19
- Position
- chr3:196,669,545-196,670,414
- Genome
- hg38
- Position
- chr3:196,942,674-196,943,543
- HGNC
- HGNC:25121 HGNC
- Ensembl
- ENSG00000270170 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 4 | 0 |
Ranking
ClinVar | |
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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
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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Search word | : | |
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 |
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SYNONYM | HIAR |
SYNONYM | KRASIM |
SYNONYM | NCBP2-AS2 |
HGNC | HGNC:25121 HGNC |
Ensembl | ENSG00000270170 Ensembl |
AllianceGenome | HGNC:25121 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000602845.2 | hg38 | chr3 | 196,942,674 | 196,943,543 | 870 |
ENST00000602845.2 | hg19 | chr3 | 196,669,545 | 196,670,414 | 870 |
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