Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs139373171
- Species
- Homo sapiens
- Symbol
- rs139373171
- Category
- Variant
- Variant type
- SNP
- Overlaps
- COP1
- Location
- 1:176149051
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.176149051C>G
- HGVS.c name
- ENSEMBL:ENST00000308769.12:c.774G>C
- ENSEMBL:ENST00000367666.5:c.351G>C
- HGVS.p name
- ENSP00000310943:p.Gln258His
- ENSP00000356638:p.Gln117His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:175944831...176207286 (262.46 kb)
- Assembly version
- Not Available
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