Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs17023108
- Species
- Homo sapiens
- Symbol
- rs17023108
- Category
- Variant
- Variant type
- SNP
- Overlaps
- WARS2
- Location
- 1:119034281
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000001.11:g.119034281G>A
- HGVS.c name
- ENSEMBL:ENST00000235521.5:c.516-68C>T
- ENSEMBL:ENST00000369426.9:c.516-68C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:119031216...119140672 (109.46 kb)
- Assembly version
- Not Available
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