Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs765676819
- Species
- Homo sapiens
- Symbol
- rs765676819
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FIG4
- Location
- 6:109715125
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000006.12:g.109715125C>T
- HGVS.c name
- ENSEMBL:ENST00000230124.8:c.114C>T
- ENSEMBL:ENST00000368941.2:c.114C>T
- HGVS.p name
- ENSP00000230124:p.Val38=
- ENSP00000357937:p.Val38=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:109690609...109878098 (187.49 kb)
- Assembly version
- Not Available
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