Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs756594825
- Species
- Homo sapiens
- Symbol
- rs756594825
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ST3GAL5
- Location
- 2:85846509
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.85846509A>C
- HGVS.c name
- ENSEMBL:ENST00000306262.10:n.676T>G
- ENSEMBL:ENST00000377332.8:c.597T>G
- HGVS.p name
- ENSP00000366549:p.Thr199=
- ENSP00000377394:p.Thr211=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:85837120...85905199 (68.08 kb)
- Assembly version
- Not Available
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