Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs114506587
- Species
- Homo sapiens
- Symbol
- rs114506587
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC3A2
- Location
- 11:62881314
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- splice region variant&synonymous variant
- HGVS.g name
- NC_000011.10:g.62881314T>G
- HGVS.c name
- ENSEMBL:ENST00000338663.12:c.291T>G
- ENSEMBL:ENST00000377889.6:c.408T>G
- HGVS.p name
- ENSP00000340815:p.Ala97=
- ENSP00000367121:p.Ala136=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:62856004...62888880 (32.88 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction