Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3320019248
- Species
- Rattus norvegicus
- Symbol
- rs3320019248
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Prokr2
- Location
- 3:119632575
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051338.1:g.119632575C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000028889.3:c.572+2572G>A
- RefSeq:NM_138978.2:c.572+2572G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:119624738...119639442 (14.70 kb)
- Assembly version
- Not Available
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