Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs764589776
- Species
- Homo sapiens
- Symbol
- rs764589776
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CHCHD2
- Location
- 7:56104219
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000007.14:g.56104219T>G
- HGVS.c name
- ENSEMBL:ENST00000395422.4:c.300+7A>C
- ENSEMBL:ENST00000473095.1:n.318+7A>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:56094567...56106479 (11.91 kb)
- Assembly version
- Not Available
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