Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105577034
- Species
- Rattus norvegicus
- Symbol
- rs105577034
- Category
- Variant
- Variant type
- SNP
- Overlaps
- St3gal5
- Location
- 4:104175764
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051339.1:g.104175764T>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000050249.3:c.234+3078T>G
- ENSEMBL:ENSRNOT00000078793.2:c.315+3078T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:104134613...104192558 (57.95 kb)
- Assembly version
- Not Available
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