Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323720133
- Species
- Rattus norvegicus
- Symbol
- rs3323720133
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Aifm1
- Location
- X:127670149
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051356.1:g.127670149T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000008503.6:c.603-614A>G
- ENSEMBL:ENSRNOT00000084848.2:c.591-614A>G
- 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
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