Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs760655471
- Species
- Homo sapiens
- Symbol
- rs760655471
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BRCA2
- Location
- 13:32319099
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000013.11:g.32319099T>C
- HGVS.c name
- ENSEMBL:ENST00000470094.2:n.289T>C
- ENSEMBL:ENST00000530893.7:c.-280T>C
- HGVS.p name
- ENSP00000439902:p.Asn30=
- ENSP00000505508:p.Asn30=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:32315077...32400268 (85.19 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction