Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323726979
- Species
- Rattus norvegicus
- Symbol
- rs3323726979
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Aifm1
- Location
- X:127677204
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051356.1:g.127677204G>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000008503.6:c.246+2541C>A
- ENSEMBL:ENSRNOT00000084848.2:c.234+1306C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:127650223...127689356 (39.13 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction