Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs376638547
- Species
- Homo sapiens
- Symbol
- rs376638547
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NFATC2IP
- Location
- 16:28954583
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- NC_000016.10:g.28954583C>T
- HGVS.c name
- ENSEMBL:ENST00000320805.9:c.479C>T
- ENSEMBL:ENST00000562977.1:n.465+2379C>T
- HGVS.p name
- ENSP00000324792:p.Ser160Leu
- NP_116204:p.Ser160Leu
- 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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