Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319368619
- Species
- Rattus norvegicus
- Symbol
- rs3319368619
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gpx8
- Location
- 2:44678173
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)2:44678173C>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000013979.6:c.451+907G>C
- ENSEMBL:ENSRNOT00000115785.1:c.205-1163G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:44676448...44680195 (3.75 kb)
- Assembly version
- Not Available
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