Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201982369
- Species
- Homo sapiens
- Symbol
- rs201982369
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HIPK3
- Location
- 11:33351837
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)11:33351837A>G
- HGVS.c name
- ENSEMBL:ENST00000303296.9:c.3037A>G
- ENSEMBL:ENST00000379016.7:c.2974A>G
- HGVS.p name
- ENSP00000304226:p.Asn1013Asp
- ENSP00000368301:p.Asn992Asp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:33256672...33357023 (100.35 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction