Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1326350955
- Species
- Homo sapiens
- Symbol
- rs1326350955
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FUCA1
- Location
- 1:23848629
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)1:23848629C>T
- HGVS.c name
- ENSEMBL:ENST00000374479.4:c.1160+20G>A
- RefSeq:NM_000147.5:c.1160+20G>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
- Viewer Help
Data currently unavailable; sequence viewer under construction