Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs150208595
- Species
- Homo sapiens
- Symbol
- rs150208595
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GLTP
- Location
- 12:109852643
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000012.12:g.109852643C>T
- HGVS.c name
- ENSEMBL:ENST00000318348.9:c.542G>A
- ENSEMBL:ENST00000537066.2:n.885G>A
- HGVS.p name
- ENSP00000315263:p.Arg181His
- ENSP00000440136:p.Pro154=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:109850945...109880541 (29.60 kb)
- Assembly version
- Not Available
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