Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs373342102
- Species
- Homo sapiens
- Symbol
- rs373342102
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RADIL
- Location
- 7:4877997
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000007.14:g.4877997G>A
- HGVS.c name
- ENSEMBL:ENST00000399583.4:c.143C>T
- ENSEMBL:ENST00000445392.5:n.266C>T
- HGVS.p name
- ENSP00000382492:p.Ala48Val
- ENSP00000398057:p.Ala48Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:4797055...4883716 (86.66 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction