Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1681871908
- Species
- Homo sapiens
- Symbol
- rs1681871908
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ST3GAL5
- Location
- 2:85840361
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:85840361A>G
- HGVS.c name
- ENSEMBL:ENST00000377332.8:c.920T>C
- ENSEMBL:ENST00000393805.6:c.956T>C
- HGVS.p name
- ENSP00000366549:p.Val307Ala
- ENSP00000377394:p.Val319Ala
- 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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