Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1805337
- Species
- Homo sapiens
- Symbol
- rs1805337
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RXRA
- Location
- 9:134401726
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000009.12:g.134401726C>T
- HGVS.c name
- ENSEMBL:ENST00000356384.4:n.533C>T
- ENSEMBL:ENST00000481739.2:c.123C>T
- HGVS.p name
- ENSP00000419692:p.Ile41=
- ENSP00000497073:p.Ile71=
- 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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