Linked Data
MyVariant Identifiers:
chr19:g.855761T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.855761T>G , CM000681.2:g.855761T>G | GRCh38 |
| NC_000019.9:g.855761T>G , CM000681.1:g.855761T>G | GRCh37 |
| NC_000019.8:g.806761T>G | NCBI36 |
| NG_007274.1:g.1097T>G , LRG_46:g.1097T>G | |
| NG_009627.1:g.8471T>G , LRG_57:g.8471T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263621.2:c.564T>G MANE Select | ENSP00000263621.1:p.Thr188= | |
| ENST00000263621.1:c.564T>G | ENSP00000263621.1:p.Thr188= | |
| ENST00000590230.5:c.564T>G | ENSP00000466090.1:p.Thr188= | |
| NM_001972.2:c.564T>G , LRG_57t1:c.564T>G | NP_001963.1:p.Thr188= | |
| XM_011527775.1:c.564T>G | XP_011526077.1:p.Thr188= | |
| XM_011527776.1:c.564T>G | XP_011526078.1:p.Thr188= | |
| NM_001972.3:c.564T>G | NP_001963.1:p.Thr188= | |
| NM_001972.4:c.564T>G MANE Select | NP_001963.1:p.Thr188= |