Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs768846633
- Species
- Homo sapiens
- Symbol
- rs768846633
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ICAM1
- Location
- 19:10283549
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)19:10283549C>A
- HGVS.c name
- ENSEMBL:ENST00000264832.8:c.400C>A
- ENSEMBL:ENST00000423829.2:c.68-580C>A
- HGVS.p name
- ENSP00000264832:p.Arg134Ser
- NP_000192:p.Arg134Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:10271093...10286615 (15.52 kb)
- Assembly version
- Not Available
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