Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs866880642
- Species
- Homo sapiens
- Symbol
- rs866880642
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TXNDC9
- Location
- 2:99333075
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:99333075G>A
- HGVS.c name
- ENSEMBL:ENST00000264255.8:c.136C>T
- ENSEMBL:ENST00000409434.5:c.136C>T
- HGVS.p name
- ENSP00000264255:p.Arg46Cys
- ENSP00000386889:p.Arg46Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:99306184...99340702 (34.52 kb)
- Assembly version
- Not Available
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