AIRN antisense of IGF2R non-protein coding RNA
Information
Clinical Significance
MGeND | ClinVar | |
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Pathogenic | 1 | 0 |
Ranking
ClinVar | |
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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
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 |
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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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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 | AIR |
SYNONYM | IGF2R-AS |
SYNONYM | IGF2R-AS1 |
SYNONYM | IGF2RAS |
SYNONYM | NCRNA00088 |
MIM | 604893 OMIM |
HGNC | HGNC:34515 HGNC |
Ensembl | ENSG00000268257 Ensembl |
AllianceGenome | HGNC:34515 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000609176.1 | hg38 | chr6 | 160,003,291 | 160,007,664 | 4,374 |
ENST00000601203.1 | hg38 | chr6 | 160,003,291 | 160,007,664 | 4,374 |
ENST00000601203.1 | hg19 | chr6 | 160,424,323 | 160,428,696 | 4,374 |
ENST00000609176.1 | hg19 | chr6 | 160,424,323 | 160,428,696 | 4,374 |
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