Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105793095
- Species
- Rattus norvegicus
- Symbol
- rs105793095
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Large1
- Location
- 19:11632254
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051354.1:g.11632254T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000064105.2:c.1132-5914A>G
- ENSEMBL:ENSRNOT00000090886.2:c.1448+4131A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:11603129...12048930 (445.80 kb)
- Assembly version
- Not Available
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