C21orf91-OT1 C21orf91 overlapping transcript 1
Information
- Symbol
- C21orf91-OT1
- Type
- ncRNA
- Description
- C21orf91 overlapping transcript 1
- Entrez Gene ID
- 246312
- Genome
- hg19
- Position
- chr21:19,135,632-19,164,840
- Genome
- hg38
- Position
- chr21:17,763,315-17,792,523
- HGNC
- HGNC:16729 HGNC
- Ensembl
- ENSG00000240770 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 |
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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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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 | D21S2089E |
SYNONYM | NCRNA00285 |
HGNC | HGNC:16729 HGNC |
Ensembl | ENSG00000240770 Ensembl |
AllianceGenome | HGNC:16729 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000430815.5 | hg38 | chr21 | 17,763,315 | 17,792,523 | 29,209 |
ENST00000439392.1 | hg38 | chr21 | 17,777,404 | 17,792,509 | 15,106 |
ENST00000430815.5 | hg19 | chr21 | 19,135,632 | 19,164,840 | 29,209 |
ENST00000439392.1 | hg19 | chr21 | 19,149,721 | 19,164,826 | 15,106 |
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