Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs776016166
- Species
- Homo sapiens
- Symbol
- rs776016166
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ST3GAL5
- Location
- 2:85863439
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.85863439C>T
- HGVS.c name
- ENSEMBL:ENST00000306262.10:n.166-2147G>A
- ENSEMBL:ENST00000377332.8:c.129G>A
- HGVS.p name
- ENSP00000366549:p.Ser43=
- ENSP00000377394:p.Ser15=
- 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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