Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1138484
- Species
- Homo sapiens
- Symbol
- rs1138484
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ST3GAL5
- Location
- 2:85861188
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:85861188T>C
- HGVS.c name
- ENSEMBL:ENST00000306262.10:n.270A>G
- ENSEMBL:ENST00000377332.8:c.311A>G
- HGVS.p name
- ENSP00000366549:p.His104Arg
- ENSP00000377394:p.His76Arg
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction