Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs183153328
- Species
- Homo sapiens
- Symbol
- rs183153328
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TP53
- Location
- 17:7667908
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000017.11:g.7667908C>A
- HGVS.c name
- ENSEMBL:ENST00000359597.8:c.994-1664G>T
- ENSEMBL:ENST00000413465.6:c.783-5894G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:7661779...7687546 (25.77 kb)
- Assembly version
- Not Available
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