Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs986185258
- Species
- Homo sapiens
- Symbol
- rs986185258
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RXRA
- Location
- 9:134417311
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:134417311G>C
- HGVS.c name
- ENSEMBL:ENST00000356384.4:n.1174G>C
- ENSEMBL:ENST00000481739.2:c.764G>C
- HGVS.p name
- ENSP00000419692:p.Gly255Ala
- ENSP00000500402:p.Gly228Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:134317098...134440585 (123.49 kb)
- Assembly version
- Not Available
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