Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1554434216
- Species
- Homo sapiens
- Symbol
- rs1554434216
- Category
- Variant
- Variant type
- SNP
- Overlaps
- UBE2H
- Location
- 7:129879637
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000007.14:g.129879637A>G
- HGVS.c name
- ENSEMBL:ENST00000355621.8:c.136T>C
- ENSEMBL:ENST00000472396.5:c.136T>C
- HGVS.p name
- ENSP00000347836:p.Tyr46His
- ENSP00000417681:p.Tyr13His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:129830732...129952960 (122.23 kb)
- Assembly version
- Not Available
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