Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs368248704
- Species
- Homo sapiens
- Symbol
- rs368248704
- Category
- Variant
- Variant type
- SNP
- Overlaps
- WDR83
- Location
- 19:12669994
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000019.10:g.12669994C>G
- HGVS.c name
- ENSEMBL:ENST00000418543.8:c.121C>G
- ENSEMBL:ENST00000546754.5:n.551C>G
- HGVS.p name
- ENSP00000402653:p.Leu41Val
- NP_001093207:p.Leu41Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:12666802...12675832 (9.03 kb)
- Assembly version
- Not Available
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