Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1181275593
- Species
- Homo sapiens
- Symbol
- rs1181275593
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SNRPB2
- Location
- 20:16737384
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)20:16737384A>G
- HGVS.c name
- ENSEMBL:ENST00000246071.8:c.361A>G
- ENSEMBL:ENST00000377943.9:c.361A>G
- HGVS.p name
- ENSP00000246071:p.Asn121Asp
- ENSP00000367178:p.Asn121Asp
- 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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