Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2365338
- Species
- Homo sapiens
- Symbol
- rs2365338
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LOXHD1
- Location
- 18:46560063
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000018.10:g.46560063A>C
- HGVS.c name
- ENSEMBL:ENST00000335730.6:n.2374+20T>G
- ENSEMBL:ENST00000441551.6:c.2599-2574T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:46476961...46657220 (180.26 kb)
- Assembly version
- Not Available
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