Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs756277096
- Species
- Homo sapiens
- Symbol
- rs756277096
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RBBP9
- Location
- 20:18490436
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000020.11:g.18490436G>A
- HGVS.c name
- ENSEMBL:ENST00000337227.9:c.293C>T
- ENSEMBL:ENST00000491835.1:n.257C>T
- HGVS.p name
- ENSP00000336866:p.Ala98Val
- NP_006597:p.Ala98Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:18486540...18497225 (10.69 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction