Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs886046321
- Species
- Homo sapiens
- Symbol
- rs886046321
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FUCA1
- Location
- 1:23845171
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (GRCh38)1:23845171A>T
- HGVS.c name
- ENSEMBL:ENST00000374479.4:c.*544T>A
- RefSeq:NM_000147.5:c.*544T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:23845077...23868290 (23.21 kb)
- Assembly version
- Not Available
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