Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs769571023
- Species
- Homo sapiens
- Symbol
- rs769571023
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARIH2
- Location
- 3:48981711
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.48981711G>A
- HGVS.c name
- ENSEMBL:ENST00000356401.9:c.1309G>A
- ENSEMBL:ENST00000449376.5:c.1309G>A
- HGVS.p name
- ENSP00000348769:p.Gly437Arg
- ENSP00000403222:p.Gly437Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:48918821...48986382 (67.56 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction