Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs554831708
- Species
- Homo sapiens
- Symbol
- rs554831708
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SNCA
- Location
- 4:89828320
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000004.12:g.89828320T>A
- HGVS.c name
- ENSEMBL:ENST00000336904.7:c.122-136A>T
- ENSEMBL:ENST00000345009.8:c.122-136A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:89700345...89838315 (137.97 kb)
- Assembly version
- Not Available
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