Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2050971311
- Species
- Homo sapiens
- Symbol
- rs2050971311
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BRCA1
- Location
- 17:43047622
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)17:43047622A>T
- HGVS.c name
- ENSEMBL:ENST00000352993.7:c.2041+21T>A
- ENSEMBL:ENST00000461221.5:n.5568+21T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:43044295...43170327 (126.03 kb)
- Assembly version
- Not Available
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