Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs115835484
- Species
- Homo sapiens
- Symbol
- rs115835484
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LOXHD1
- Location
- 18:46477511
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)18:46477511C>T
- HGVS.c name
- ENSEMBL:ENST00000300591.11:c.3307+143G>A
- ENSEMBL:ENST00000398686.8:c.1500G>A
- HGVS.p name
- ENSP00000381676:p.Gly500=
- ENSP00000387621:p.Gly2055=
- 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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