Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201825898
- Species
- Homo sapiens
- Symbol
- rs201825898
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRPV2
- Location
- 17:16427514
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.16427514C>G
- HGVS.c name
- ENSEMBL:ENST00000338560.12:c.1317C>G
- RefSeq:XM_005256678.6:c.1317C>G
- HGVS.p name
- ENSP00000342222:p.Ile439Met
- XP_005256735:p.Ile439Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:16415571...16437003 (21.43 kb)
- Assembly version
- Not Available
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