Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1645502822
- Species
- Homo sapiens
- Symbol
- rs1645502822
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIAA2013
- Location
- 1:11925784
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.11925784C>T
- HGVS.c name
- ENSEMBL:ENST00000376572.8:c.454G>A
- ENSEMBL:ENST00000376576.3:c.454G>A
- HGVS.p name
- ENSP00000365756:p.Val152Met
- ENSP00000365760:p.Val152Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:11919591...11926428 (6.84 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction