Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3320810739
- Species
- Rattus norvegicus
- Symbol
- rs3320810739
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Wdcp
- Location
- 6:27864196
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)6:27864196T>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000075574.3:c.1822-545T>A
- ENSEMBL:ENSRNOT00000110968.1:c.1937-606T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:27850684...27865540 (14.86 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction