MCM3AP-AS1 MCM3AP antisense RNA 1
Information
- Symbol
- MCM3AP-AS1
- Type
- ncRNA
- Description
- MCM3AP antisense RNA 1
- Entrez Gene ID
- 114044
- Genome
- hg19
- Position
- chr21:47,649,143-47,666,206
- Genome
- hg38
- Position
- chr21:46,229,229-46,246,292
- HGNC
- HGNC:16417 HGNC
- Ensembl
- ENSG00000215424 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 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 |
Search Word
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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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 |
---|---|
SYNONYM | C21orf85 |
SYNONYM | MCM3AP-AS |
SYNONYM | MCM3APAS |
SYNONYM | MCM3APASB |
SYNONYM | NCRNA00031 |
HGNC | HGNC:16417 HGNC |
Ensembl | ENSG00000215424 Ensembl |
AllianceGenome | HGNC:16417 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000414659.5 | hg38 | chr21 | 46,229,231 | 46,251,701 | 22,471 |
ENST00000662666.1 | hg38 | chr21 | 46,229,266 | 46,251,725 | 22,460 |
ENST00000432735.5 | hg38 | chr21 | 46,229,234 | 46,242,999 | 13,766 |
ENST00000656253.1 | hg38 | chr21 | 46,229,224 | 46,251,745 | 22,522 |
ENST00000664725.1 | hg38 | chr21 | 46,229,229 | 46,246,292 | 17,064 |
ENST00000669476.1 | hg38 | chr21 | 46,229,221 | 46,251,871 | 22,651 |
ENST00000669476.1 | hg19 | chr21 | 47,649,135 | 47,671,785 | 22,651 |
ENST00000656253.1 | hg19 | chr21 | 47,649,138 | 47,671,659 | 22,522 |
ENST00000664725.1 | hg19 | chr21 | 47,649,143 | 47,666,206 | 17,064 |
ENST00000414659.5 | hg19 | chr21 | 47,649,145 | 47,671,615 | 22,471 |
ENST00000432735.5 | hg19 | chr21 | 47,649,148 | 47,662,913 | 13,766 |
ENST00000662666.1 | hg19 | chr21 | 47,649,180 | 47,671,639 | 22,460 |
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