Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201796393
- Species
- Homo sapiens
- Symbol
- rs201796393
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ACTR8
- Location
- 3:53872524
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant&splice region variant
- HGVS.g name
- NC_000003.12:g.53872524C>A
- HGVS.c name
- ENSEMBL:ENST00000335754.8:c.1162G>T
- ENSEMBL:ENST00000482349.5:c.829G>T
- HGVS.p name
- ENSP00000336842:p.Ala388Ser
- ENSP00000417230:p.Arg141Ser
- 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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