Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1851244921
- Species
- Homo sapiens
- Symbol
- rs1851244921
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HRAS
- Location
- 11:533539
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000011.10:g.533539C>T
- HGVS.c name
- ENSEMBL:ENST00000397594.7:c.364G>A
- ENSEMBL:ENST00000397596.6:c.364G>A
- HGVS.p name
- ENSP00000380722:p.Ala122Thr
- ENSP00000380723:p.Ala122Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:532242...537321 (5.08 kb)
- Assembly version
- Not Available
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