Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200719828
- Species
- Homo sapiens
- Symbol
- rs200719828
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IQCB1
- Location
- 3:121770547
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:121770547C>T
- HGVS.c name
- ENSEMBL:ENST00000310864.11:c.1595G>A
- ENSEMBL:ENST00000349820.10:c.1196G>A
- HGVS.p name
- ENSP00000311505:p.Gly532Glu
- ENSP00000323756:p.Gly399Glu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:121769761...121835079 (65.32 kb)
- Assembly version
- Not Available
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