Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323419877
- Species
- Rattus norvegicus
- Symbol
- rs3323419877
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2f4
- Location
- 19:33180243
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051354.1:g.33180243A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000021145.8:c.1049-362A>G
- RefSeq:NM_001271345.1:c.1031-362A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:33174396...33181806 (7.41 kb)
- Assembly version
- Not Available
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