Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs197653188
- Species
- Rattus norvegicus
- Symbol
- rs197653188
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Lmo4
- Location
- 2:233274351
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051337.1:g.233274351G>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000067502.3:c.236+3156C>A
- RefSeq:NM_001009708.1:c.236+3156C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:233264180...233280881 (16.70 kb)
- Assembly version
- Not Available
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