Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1950029767
- Species
- Homo sapiens
- Symbol
- rs1950029767
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HAL
- Location
- 12:95995847
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000012.12:g.95995847G>A
- HGVS.c name
- ENSEMBL:ENST00000261208.8:c.64C>T
- ENSEMBL:ENST00000538703.5:c.64C>T
- HGVS.p name
- ENSP00000261208:p.Leu22Phe
- ENSP00000440861:p.Leu22Phe
- 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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