Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs556456151
- Species
- Homo sapiens
- Symbol
- rs556456151
- Category
- Variant
- Variant type
- SNP
- Overlaps
- P2RX5
- Location
- 17:3688017
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- NC_000017.11:g.3688017C>G
- HGVS.c name
- ENSEMBL:ENST00000345901.7:c.904G>C
- ENSEMBL:ENST00000547178.5:c.973G>C
- HGVS.p name
- ENSP00000342161:p.Gly302Arg
- ENSP00000447545:p.Gly301Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:3672199...3723835 (51.64 kb)
- Assembly version
- Not Available
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