Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106787278
- Species
- Rattus norvegicus
- Symbol
- rs106787278
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ctrb1
- Location
- 19:39654813
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051354.1:g.39654813T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000026017.5:c.316-88A>G
- ENSEMBL:ENSRNOT00000115260.1:c.349-88A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:39652931...39657689 (4.76 kb)
- Assembly version
- Not Available
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