Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198073111
- Species
- Rattus norvegicus
- Symbol
- rs198073111
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sv2a
- Location
- 2:183750314
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051337.1:g.183750314G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000028760.5:c.1379+164G>A
- RefSeq:NM_057210.3:c.1379+164G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:183741489...183757290 (15.80 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction