Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs889466758
- Species
- Homo sapiens
- Symbol
- rs889466758
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CPLX3
- Location
- 15:74828080
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000015.10:g.74828080A>G
- HGVS.c name
- ENSEMBL:ENST00000395018.6:c.211A>G
- RefSeq:NM_001030005.3:c.211A>G
- HGVS.p name
- ENSP00000378464:p.Thr71Ala
- NP_001025176:p.Thr71Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:74826627...74831802 (5.18 kb)
- Assembly version
- Not Available
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