Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3320673838
- Species
- Rattus norvegicus
- Symbol
- rs3320673838
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Nipal3
- Location
- 5:147692122
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051340.1:g.147692122A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000025075.7:c.965-903T>C
- ENSEMBL:ENSRNOT00000109539.1:c.1034-903T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:147685288...147726351 (41.06 kb)
- Assembly version
- Not Available
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