Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323525332
- Species
- Rattus norvegicus
- Symbol
- rs3323525332
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Arid5b
- Location
- 20:20440255
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051355.1:g.20440255T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000000787.9:c.734-6669T>C
- RefSeq:NM_001107624.1:c.734-6669T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:20307731...20490746 (183.02 kb)
- Assembly version
- Not Available
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