Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs223709888
- Species
- Mus musculus
- Symbol
- rs223709888
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Myl6b
- Location
- 10:128333432
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000076.7:g.128333432C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000026428.1:c.-46-146G>A
- RefSeq:NM_172259.1:c.-46-146G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:128330026...128334554 (4.53 kb)
- Assembly version
- Not Available
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