MIR892A microRNA 892a
Information
- Symbol
- MIR892A
- Type
- ncRNA
- Description
- microRNA 892a
- Entrez Gene ID
- 100126342
- Genome
- hg19
- Position
- chrX:145,078,187-145,078,261
- Genome
- hg38
- Position
- chrX:145,996,669-145,996,743
- HGNC
- HGNC:33639 HGNC
- Ensembl
- ENSG00000215943 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 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 | MIRN892A |
HGNC | HGNC:33639 HGNC |
Ensembl | ENSG00000215943 Ensembl |
miRBase | MI0005528 |
AllianceGenome | HGNC:33639 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000401124.1 | hg38 | chrX | 145,996,669 | 145,996,743 | 75 |
ENST00000401124.1 | hg19 | chrX | 145,078,187 | 145,078,261 | 75 |
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