Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs775632661
- Species
- Homo sapiens
- Symbol
- rs775632661
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARIH2
- Location
- 3:48970646
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.48970646C>T
- HGVS.c name
- ENSEMBL:ENST00000356401.9:c.712C>T
- ENSEMBL:ENST00000449376.5:c.712C>T
- HGVS.p name
- ENSP00000348769:p.Arg238Trp
- ENSP00000403222:p.Arg238Trp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:48918821...48986382 (67.56 kb)
- Assembly version
- Not Available
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