Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1326280728
- Species
- Homo sapiens
- Symbol
- rs1326280728
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRPV2
- Location
- 17:16433681
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.16433681T>A
- HGVS.c name
- ENSEMBL:ENST00000338560.12:c.2097T>A
- ENSEMBL:ENST00000475513.5:n.450T>A
- HGVS.p name
- ENSP00000342222:p.Asp699Glu
- ENSP00000465609:p.Asp118Glu
- 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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