Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs776576177
- Species
- Homo sapiens
- Symbol
- rs776576177
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HMGB2
- Location
- 4:173332143
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.173332143A>C
- HGVS.c name
- ENSEMBL:ENST00000296503.10:c.567T>G
- ENSEMBL:ENST00000438704.6:c.567T>G
- HGVS.p name
- ENSP00000296503:p.Asp189Glu
- ENSP00000393448:p.Asp189Glu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:173331376...173334432 (3.06 kb)
- Assembly version
- Not Available
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