Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs4252589
- Species
- Homo sapiens
- Symbol
- rs4252589
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HSPB2
- Location
- 11:111913677
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- (GRCh38)11:111913677G>A
- HGVS.c name
- ENSEMBL:ENST00000304298.4:c.331G>A
- ENSEMBL:ENST00000527616.1:n.425G>A
- HGVS.p name
- ENSP00000302476:p.Gly111Ser
- NP_001532:p.Gly111Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:111912734...111914093 (1.36 kb)
- Assembly version
- Not Available
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