Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs11831226
- Species
- Homo sapiens
- Symbol
- rs11831226
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MMAB
- Location
- 12:109556307
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (GRCh38)12:109556307A>C
- HGVS.c name
- ENSEMBL:ENST00000545712.7:c.*721T>G
- RefSeq:NM_052845.4:c.*721T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:109553715...109573580 (19.87 kb)
- Assembly version
- Not Available
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