Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs8009030
- Species
- Homo sapiens
- Symbol
- rs8009030
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NUBPL
- Location
- 14:31850365
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)14:31850365A>G
- HGVS.c name
- ENSEMBL:ENST00000281081.12:c.897+164A>G
- ENSEMBL:ENST00000418681.6:n.619+164A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:31489956...31861224 (371.27 kb)
- Assembly version
- Not Available
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