Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs886706741
- Species
- Homo sapiens
- Symbol
- rs886706741
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NFATC2IP
- Location
- 16:28951091
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)16:28951091G>C
- HGVS.c name
- ENSEMBL:ENST00000320805.9:c.80G>C
- ENSEMBL:ENST00000562977.1:n.85G>C
- HGVS.p name
- ENSP00000324792:p.Gly27Ala
- NP_116204:p.Gly27Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:28950807...28967092 (16.29 kb)
- Assembly version
- Not Available
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