Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs197029262
- Species
- Rattus norvegicus
- Symbol
- rs197029262
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Arcn1
- Location
- 8:45073217
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051343.1:g.45073217T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000082687.2:c.267+381A>G
- ENSEMBL:ENSRNOT00000102084.1:c.267+381A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:45057617...45082247 (24.63 kb)
- Assembly version
- Not Available
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