Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs972179032
- Species
- Homo sapiens
- Symbol
- rs972179032
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRK1
- Location
- 15:101026060
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000015.10:g.101026060C>T
- HGVS.c name
- ENSEMBL:ENST00000388948.8:c.2328C>T
- RefSeq:NM_024652.6:c.2328C>T
- HGVS.p name
- ENSP00000373600:p.Ala776=
- NP_078928:p.Ala776=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:100919327...101078257 (158.93 kb)
- Assembly version
- Not Available
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