Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201990827
- Species
- Homo sapiens
- Symbol
- rs201990827
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EXOSC5
- Location
- 19:41391846
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000019.10:g.41391846C>G
- HGVS.c name
- ENSEMBL:ENST00000221233.9:c.379G>C
- ENSEMBL:ENST00000593523.2:n.413G>C
- HGVS.p name
- ENSP00000221233:p.Gly127Arg
- ENSP00000471002:p.Gly89Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:41386371...41397362 (10.99 kb)
- Assembly version
- Not Available
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