Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs886053173
- Species
- Homo sapiens
- Symbol
- rs886053173
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRIM37
- Location
- 17:58998996
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- NC_000017.11:g.58998996A>G
- HGVS.c name
- ENSEMBL:ENST00000262294.12:c.*381T>C
- ENSEMBL:ENST00000393065.6:c.*381T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:58967201...59106921 (139.72 kb)
- Assembly version
- Not Available
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