Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319565069
- Species
- Rattus norvegicus
- Symbol
- rs3319565069
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sv2a
- Location
- 2:183756053
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)2:183756053C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000028760.5:c.*341C>T
- RefSeq:NM_057210.3:c.*341C>T
- 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
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