Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1319989898
- Species
- Homo sapiens
- Symbol
- rs1319989898
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EMC3
- Location
- 3:9986547
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:9986547G>C
- HGVS.c name
- ENSEMBL:ENST00000245046.7:c.115C>G
- ENSEMBL:ENST00000429759.5:n.136C>G
- HGVS.p name
- ENSP00000245046:p.Gln39Glu
- ENSP00000474771:p.Gln39Glu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:9962682...10011202 (48.52 kb)
- Assembly version
- Not Available
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