Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1568276547
- Species
- Homo sapiens
- Symbol
- rs1568276547
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KDSR
- Location
- 18:63338903
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)18:63338903T>A
- HGVS.c name
- ENSEMBL:ENST00000326575.9:c.502-20A>T
- ENSEMBL:ENST00000586791.5:n.2122-20A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:63327726...63367228 (39.50 kb)
- Assembly version
- Not Available
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