Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2102473665
- Species
- Homo sapiens
- Symbol
- rs2102473665
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EFNA1
- Location
- 1:155134023
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:155134023T>C
- HGVS.c name
- ENSEMBL:ENST00000368406.2:c.508T>C
- ENSEMBL:ENST00000368407.8:c.574T>C
- HGVS.p name
- ENSP00000357391:p.Trp170Arg
- ENSP00000357392:p.Trp192Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:155127876...155134899 (7.02 kb)
- Assembly version
- Not Available
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