Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105029884
- Species
- Rattus norvegicus
- Symbol
- rs105029884
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Hnrnph3
- Location
- 20:25622842
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051355.1:g.25622842A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000032600.6:c.568+5A>C
- ENSEMBL:ENSRNOT00000073617.3:c.*123+5A>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:25614733...25625814 (11.08 kb)
- Assembly version
- Not Available
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