Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs771450050
- Species
- Homo sapiens
- Symbol
- rs771450050
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EFNA1
- Location
- 1:155133973
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:155133973T>C
- HGVS.c name
- ENSEMBL:ENST00000368406.2:c.458T>C
- ENSEMBL:ENST00000368407.8:c.524T>C
- HGVS.p name
- ENSP00000357391:p.Val153Ala
- ENSP00000357392:p.Val175Ala
- 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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