Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs196972521
- Species
- Rattus norvegicus
- Symbol
- rs196972521
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Onecut2
- Location
- 18:57869849
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051353.1:g.57869849T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000078378.2:c.1232-8838T>C
- RefSeq:NM_001400633.1:c.1232-8838T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:57831647...57890884 (59.24 kb)
- Assembly version
- Not Available
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