Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs186840501
- Species
- Homo sapiens
- Symbol
- rs186840501
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HAL
- Location
- 12:95973804
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (GRCh38)12:95973804G>C
- HGVS.c name
- ENSEMBL:ENST00000261208.8:c.*428C>G
- ENSEMBL:ENST00000541929.5:c.*428C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:95972662...95996365 (23.70 kb)
- Assembly version
- Not Available
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