Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319641959
- Species
- Rattus norvegicus
- Symbol
- rs3319641959
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sv2a
- Location
- 2:183752082
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)2:183752082C>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000028760.5:c.1678+792C>G
- RefSeq:NM_057210.3:c.1678+792C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:183741489...183757290 (15.80 kb)
- Assembly version
- Not Available
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