Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs207478526
- Species
- Homo sapiens
- Symbol
- rs207478526
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DACH2
- Location
- X:86269046
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000023.11:g.86269046G>T
- HGVS.c name
- ENSEMBL:ENST00000373125.9:c.489-107778G>T
- ENSEMBL:ENST00000373131.5:c.488+119938G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:86148451...86832604 (684.15 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction