Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs46987328
- Species
- Mus musculus
- Symbol
- rs46987328
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Dmd
- Location
- X:82577933
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)X:82577933C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000114000.1:c.649+44382C>T
- RefSeq:NM_007868.6:c.649+44382C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:81992476...84249747 (2,257.27 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction