Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs748287780
- Species
- Homo sapiens
- Symbol
- rs748287780
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RBBP9
- Location
- 20:18489793
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)20:18489793C>T
- HGVS.c name
- ENSEMBL:ENST00000337227.9:c.532G>A
- ENSEMBL:ENST00000491835.1:n.496G>A
- HGVS.p name
- ENSP00000336866:p.Val178Ile
- NP_006597:p.Val178Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:18486540...18497225 (10.69 kb)
- Assembly version
- Not Available
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