Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs211813784
- Species
- Mus musculus
- Symbol
- rs211813784
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Krt12
- Location
- 11:99307937
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000077.7:g.99307937C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000017741.1:c.1296-146G>A
- RefSeq:NM_010661.2:c.1296-146G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:99306492...99313085 (6.59 kb)
- Assembly version
- Not Available
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