Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1328953759
- Species
- Homo sapiens
- Symbol
- rs1328953759
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ALDH6A1
- Location
- 14:74067566
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.74067566C>A
- HGVS.c name
- ENSEMBL:ENST00000350259.8:c.817G>T
- ENSEMBL:ENST00000492026.4:n.1379+10308C>A
- HGVS.p name
- ENSP00000342564:p.Ala273Ser
- ENSP00000450436:p.Ala286Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:74056847...74084492 (27.65 kb)
- Assembly version
- Not Available
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