SMC2-DT SMC2 divergent transcript
Information
- Symbol
- SMC2-DT
- Type
- ncRNA
- Description
- SMC2 divergent transcript
- Entrez Gene ID
- 101928550
- Genome
- hg19
- Position
- chr9:106,842,305-106,854,755
- Genome
- hg38
- Position
- chr9:104,080,024-104,092,474
- HGNC
- HGNC:50827 HGNC
- Ensembl
- ENSG00000270332 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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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 | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| 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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| Category | : |
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| Filtering | : |
| 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 | SMC2-AS1 |
| HGNC | HGNC:50827 HGNC |
| Ensembl | ENSG00000270332 Ensembl |
| AllianceGenome | HGNC:50827 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000603487.1 | hg38 | chr9 | 104,080,024 | 104,092,474 | 12,451 |
| ENST00000691653.1 | hg38 | chr9 | 104,077,308 | 104,091,855 | 14,548 |
| ENST00000691653.1 | hg19 | chr9 | 106,839,589 | 106,854,136 | 14,548 |
| ENST00000603487.1 | hg19 | chr9 | 106,842,305 | 106,854,755 | 12,451 |
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