Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs61757559
- Species
- Homo sapiens
- Symbol
- rs61757559
- Category
- Variant
- Variant type
- SNP
- Overlaps
- AKNA
- Location
- 9:114355965
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:114355965T>C
- HGVS.c name
- ENSEMBL:ENST00000223791.7:c.1398A>G
- ENSEMBL:ENST00000307564.8:c.3018A>G
- HGVS.p name
- ENSP00000223791:p.Ala466=
- ENSP00000303769:p.Ala1006=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:114330504...114398472 (67.97 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction