Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs146771169
- Species
- Homo sapiens
- Symbol
- rs146771169
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SNRPB2
- Location
- 20:16740846
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- splice region variant&synonymous variant
- HGVS.g name
- (GRCh38)20:16740846G>A
- HGVS.c name
- ENSEMBL:ENST00000246071.8:c.519G>A
- ENSEMBL:ENST00000377943.9:c.519G>A
- HGVS.p name
- ENSP00000246071:p.Gln173=
- ENSP00000367178:p.Gln173=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:16729961...16742564 (12.60 kb)
- Assembly version
- Not Available
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