Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1371251341
- Species
- Homo sapiens
- Symbol
- rs1371251341
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ICAM1
- Location
- 19:10274921
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000019.10:g.10274921A>G
- HGVS.c name
- ENSEMBL:ENST00000264832.8:c.224A>G
- ENSEMBL:ENST00000423829.2:c.67+3695A>G
- HGVS.p name
- ENSP00000264832:p.Asn75Ser
- ENSP00000465680:p.Asn75Ser
- 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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