Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs143862755
- Species
- Homo sapiens
- Symbol
- rs143862755
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HDHD2
- Location
- 18:47130304
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)18:47130304G>A
- HGVS.c name
- ENSEMBL:ENST00000300605.11:c.335C>T
- ENSEMBL:ENST00000586546.5:n.535+4192C>T
- HGVS.p name
- ENSP00000300605:p.Ala112Val
- ENSP00000465282:p.Ala103Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:47107408...47150500 (43.09 kb)
- Assembly version
- Not Available
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