Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1026600064
- Species
- Homo sapiens
- Symbol
- rs1026600064
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FBXO11
- Location
- 2:47808355
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (GRCh38)2:47808355A>G
- HGVS.c name
- ENSEMBL:ENST00000402508.5:c.2376T>C
- ENSEMBL:ENST00000403359.8:c.2628T>C
- HGVS.p name
- ENSP00000384823:p.His876=
- ENSP00000385127:p.His30=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:47789316...47906498 (117.18 kb)
- Assembly version
- Not Available
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