Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs201389692
- Species
- Homo sapiens
- Symbol
- rs201389692
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TARBP1
- Location
- 1:234401239
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.234401239C>T
- HGVS.c name
- ENSEMBL:ENST00000040877.2:c.4013G>A
- ENSEMBL:ENST00000462259.5:n.502G>A
- HGVS.p name
- ENSP00000040877:p.Arg1338His
- NP_005637:p.Arg1338His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:234391313...234479179 (87.87 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction