Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs144565971
- Species
- Homo sapiens
- Symbol
- rs144565971
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HIPK3
- Location
- 11:33337138
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)11:33337138T>A
- HGVS.c name
- ENSEMBL:ENST00000303296.9:c.1285T>A
- ENSEMBL:ENST00000379016.7:c.1285T>A
- HGVS.p name
- ENSP00000304226:p.Ser429Thr
- ENSP00000368301:p.Ser429Thr
- 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
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