Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs5030381
- Species
- Homo sapiens
- Symbol
- rs5030381
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ICAM1
- Location
- 19:10284232
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000019.10:g.10284232C>T
- HGVS.c name
- ENSEMBL:ENST00000264832.8:c.837C>T
- ENSEMBL:ENST00000423829.2:c.171C>T
- HGVS.p name
- ENSP00000264832:p.Thr279=
- ENSP00000413124:p.Thr57=
- 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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