Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322661011
- Species
- Rattus norvegicus
- Symbol
- rs3322661011
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Nefh
- Location
- 14:79836138
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051349.1:g.79836138G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000011604.5:c.1084-18C>T
- ENSEMBL:ENSRNOT00000110325.1:c.1084-18C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:79830362...79840351 (9.99 kb)
- Assembly version
- Not Available
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