Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs214608263
- Species
- Mus musculus
- Symbol
- rs214608263
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Mybl2
- Location
- 2:162897035
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)2:162897035C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000018005.1:c.20+267C>T
- RefSeq:NM_008652.2:c.20+267C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:162896607...162926608 (30.00 kb)
- Assembly version
- Not Available
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