Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs753881759
- Species
- Homo sapiens
- Symbol
- rs753881759
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CHCHD2
- Location
- 7:56104448
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000007.14:g.56104448G>A
- HGVS.c name
- ENSEMBL:ENST00000395422.4:c.78C>T
- ENSEMBL:ENST00000473095.1:n.96C>T
- HGVS.p name
- ENSP00000378812:p.Pro26=
- ENSP00000520614:p.Pro26=
- 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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