Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1371974169
- Species
- Homo sapiens
- Symbol
- rs1371974169
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HRAS
- Location
- 11:533846
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)11:533846C>T
- HGVS.c name
- ENSEMBL:ENST00000397594.7:c.210G>A
- ENSEMBL:ENST00000397596.6:c.210G>A
- HGVS.p name
- :p.Gln70=
- ENSP00000380722:p.Gln70=
- 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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