Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs749971767
- Species
- Homo sapiens
- Symbol
- rs749971767
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ALDH6A1
- Location
- 14:74084401
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- NC_000014.9:g.74084401C>T
- HGVS.c name
- ENSEMBL:ENST00000350259.8:c.-7G>A
- ENSEMBL:ENST00000553458.6:c.-7G>A
- HGVS.p name
- Not Available
- 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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