Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321672412
- Species
- Rattus norvegicus
- Symbol
- rs3321672412
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Fhl2
- Location
- 9:45407971
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)9:45407971T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000023014.4:c.157-1020A>G
- ENSEMBL:ENSRNOT00000101412.1:c.157-1020A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:45388979...45462421 (73.44 kb)
- Assembly version
- Not Available
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