Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2079372606
- Species
- Homo sapiens
- Symbol
- rs2079372606
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ANO10
- Location
- 3:43549777
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)3:43549777C>T
- HGVS.c name
- ENSEMBL:ENST00000292246.8:c.1740G>A
- ENSEMBL:ENST00000350459.8:c.1170G>A
- HGVS.p name
- ENSP00000292246:p.Val580=
- ENSP00000327767:p.Val390=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:43354859...43691594 (336.74 kb)
- Assembly version
- Not Available
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