Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3323379739
- Species
- Rattus norvegicus
- Symbol
- rs3323379739
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Large1
- Location
- 19:11833116
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (mRatBN7.2)19:11833116G>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000064105.2:c.126C>G
- ENSEMBL:ENSRNOT00000090886.2:c.126C>G
- HGVS.p name
- ENSRNOP00000059410:p.Leu42=
- ENSRNOP00000073641:p.Leu42=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:11603129...12048930 (445.80 kb)
- Assembly version
- Not Available
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