Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323287145
- Species
- Rattus norvegicus
- Symbol
- rs3323287145
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Vps4a
- Location
- 19:34938486
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)19:34938486C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000050612.6:c.241-1643C>T
- RefSeq:NM_145678.2:c.22-1643C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:34934961...34948888 (13.93 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction