Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs780348427
- Species
- Homo sapiens
- Symbol
- rs780348427
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TPRKB
- Location
- 2:73734434
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.73734434T>C
- HGVS.c name
- ENSEMBL:ENST00000272424.11:c.136A>G
- ENSEMBL:ENST00000462166.1:n.146+94A>G
- HGVS.p name
- ENSP00000272424:p.Thr46Ala
- NP_001317317:p.Thr46Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:73729104...73737400 (8.30 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction