Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs376960198
- Species
- Homo sapiens
- Symbol
- rs376960198
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GLMN
- Location
- 1:92247095
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000001.11:g.92247095C>T
- HGVS.c name
- ENSEMBL:ENST00000370360.8:c.1635G>A
- ENSEMBL:ENST00000471465.1:n.581G>A
- HGVS.p name
- ENSP00000359385:p.Glu545=
- ENSP00000469157:p.Glu286=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:92246402...92370844 (124.44 kb)
- Assembly version
- Not Available
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