Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319041539
- Species
- Rattus norvegicus
- Symbol
- rs3319041539
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sv2b
- Location
- 1:129031733
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051336.1:g.129031733T>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000015084.7:c.452-8972A>C
- RefSeq:NM_057207.3:c.452-8972A>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:128978471...129152479 (174.01 kb)
- Assembly version
- Not Available
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