Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1342686707
- Species
- Homo sapiens
- Symbol
- rs1342686707
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SNCA
- Location
- 4:89835562
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:89835562C>G
- HGVS.c name
- ENSEMBL:ENST00000336904.7:c.106G>C
- ENSEMBL:ENST00000345009.8:c.106G>C
- HGVS.p name
- ENSP00000338345:p.Gly36Arg
- ENSP00000343683:p.Gly36Arg
- 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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