Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs371924871
- Species
- Homo sapiens
- Symbol
- rs371924871
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRCC1
- Location
- 8:85107306
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000008.11:g.85107306C>T
- HGVS.c name
- ENSEMBL:ENST00000360375.8:c.11C>T
- ENSEMBL:ENST00000517875.5:n.69C>T
- HGVS.p name
- ENSP00000353538:p.Ala4Val
- NP_208325:p.Ala4Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:85107215...85146080 (38.87 kb)
- Assembly version
- Not Available
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