Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3320637767
- Species
- Rattus norvegicus
- Symbol
- rs3320637767
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2f2
- Location
- 5:148413376
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_051340.1:g.148413376C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000072618.3:c.996C>T
- RefSeq:XM_017593850.3:c.339C>T
- HGVS.p name
- ENSRNOP00000067839:p.Cys332=
- XP_017449339:p.Cys113=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:148399193...148422595 (23.40 kb)
- Assembly version
- Not Available
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