Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs750096434
- Species
- Homo sapiens
- Symbol
- rs750096434
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NME9
- Location
- 3:138273015
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.138273015A>G
- HGVS.c name
- ENSEMBL:ENST00000317876.8:c.746-10429T>C
- ENSEMBL:ENST00000383180.6:c.746-10429T>C
- HGVS.p name
- ENSP00000417049:p.Ser437Gly
- ENSP00000417304:p.Ser468Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:138261436...138329886 (68.45 kb)
- Assembly version
- Not Available
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