Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs6504593
- Species
- Homo sapiens
- Symbol
- rs6504593
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IGF2BP1
- Location
- 17:49055457
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- NC_000017.11:g.49055457T>C
- HGVS.c name
- ENSEMBL:ENST00000290341.8:c.*6013T>C
- RefSeq:XM_047435142.1:c.*6013T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:48996558...49056145 (59.59 kb)
- Assembly version
- Not Available
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