Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319778467
- Species
- Rattus norvegicus
- Symbol
- rs3319778467
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Golga2l1
- Location
- 3:13034085
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051338.1:g.13034085A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000070863.3:c.243+141A>G
- ENSEMBL:ENSRNOT00000114551.1:c.534-259T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:13033431...13040798 (7.37 kb)
- Assembly version
- Not Available
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