Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2108855383
- Species
- Homo sapiens
- Symbol
- rs2108855383
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IL1RAP
- Location
- 3:190644353
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.190644353T>C
- HGVS.c name
- ENSEMBL:ENST00000072516.7:c.1157T>C
- ENSEMBL:ENST00000317757.8:c.1157T>C
- HGVS.p name
- ENSP00000072516:p.Val386Ala
- ENSP00000314807:p.Val386Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:190514051...190659750 (145.70 kb)
- Assembly version
- Not Available
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