Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197013707
- Species
- Rattus norvegicus
- Symbol
- rs197013707
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cmpk2
- Location
- 6:43080442
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051341.1:g.43080442A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000052003.6:c.992+910A>G
- RefSeq:NM_001108017.1:c.902+910A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:43073706...43085183 (11.48 kb)
- Assembly version
- Not Available
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