Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs761315684
- Species
- Homo sapiens
- Symbol
- rs761315684
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ACTR8
- Location
- 3:53868765
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.53868765C>T
- HGVS.c name
- ENSEMBL:ENST00000335754.8:c.1829G>A
- ENSEMBL:ENST00000482349.5:c.1496G>A
- HGVS.p name
- ENSP00000336842:p.Arg610His
- ENSP00000417230:p.Ala364Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:53858992...53882152 (23.16 kb)
- Assembly version
- Not Available
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