Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321695821
- Species
- Rattus norvegicus
- Symbol
- rs3321695821
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Clul1
- Location
- 9:113365135
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)9:113365135C>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000089735.2:c.255+2041G>C
- RefSeq:NM_001033071.1:c.255+2041G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:113344501...113370077 (25.58 kb)
- Assembly version
- Not Available
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