Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3323129534
- Species
- Rattus norvegicus
- Symbol
- rs3323129534
- Category
- Variant
- Variant type
- SNP
- Overlaps
- P4ha1
- Location
- 20:27351812
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)20:27351812A>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000070897.2:c.*287A>T
- ENSEMBL:ENSRNOT00000100609.1:c.*260+27A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:27302046...27352786 (50.74 kb)
- Assembly version
- Not Available
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