Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs752001793
- Species
- Homo sapiens
- Symbol
- rs752001793
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GLTP
- Location
- 12:109852629
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:109852629T>C
- HGVS.c name
- ENSEMBL:ENST00000318348.9:c.556A>G
- ENSEMBL:ENST00000537066.2:n.899A>G
- HGVS.p name
- ENSP00000315263:p.Asn186Asp
- ENSP00000440136:p.Gln159Arg
- 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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