Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1036793200
- Species
- Homo sapiens
- Symbol
- rs1036793200
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC3A2
- Location
- 11:62881456
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000011.10:g.62881456A>G
- HGVS.c name
- ENSEMBL:ENST00000338663.12:c.424+9A>G
- ENSEMBL:ENST00000377889.6:c.541+9A>G
- HGVS.p name
- Not Available
- 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