Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs34049091
- Species
- Homo sapiens
- Symbol
- rs34049091
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIF25
- Location
- 6:168030801
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.168030801G>A
- HGVS.c name
- ENSEMBL:ENST00000351261.4:c.121G>A
- ENSEMBL:ENST00000354419.6:c.121G>A
- HGVS.p name
- ENSP00000252688:p.Ala41Thr
- ENSP00000346401:p.Ala41Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:167996241...168045091 (48.85 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction