Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs145190179
- Species
- Homo sapiens
- Symbol
- rs145190179
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CHCHD2
- Location
- 7:56104432
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000007.14:g.56104432C>G
- HGVS.c name
- ENSEMBL:ENST00000395422.4:c.94G>C
- ENSEMBL:ENST00000473095.1:n.112G>C
- HGVS.p name
- ENSP00000378812:p.Ala32Pro
- ENSP00000520614:p.Ala32Pro
- 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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