Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs107336021
- Species
- Rattus norvegicus
- Symbol
- rs107336021
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Prpf38b
- Location
- 2:196556831
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051337.1:g.196556831A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000027738.6:c.559-1085T>C
- ENSEMBL:ENSRNOT00000104883.1:c.559-1085T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:196553224...196562271 (9.05 kb)
- Assembly version
- Not Available
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