Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs74062580
- Species
- Homo sapiens
- Symbol
- rs74062580
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ALDH6A1
- Location
- 14:74084394
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- start lost
- HGVS.g name
- (GRCh38)14:74084394T>C
- HGVS.c name
- ENSEMBL:ENST00000350259.8:c.1A>G
- ENSEMBL:ENST00000553458.6:c.1A>G
- HGVS.p name
- ENSP00000342564:p.Met1?
- ENSP00000450436:p.Met1?
- 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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