Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7529602A>T , CM000681.2:g.7529602A>T | GRCh38 |
| NC_000019.9:g.7594488A>T , CM000681.1:g.7594488A>T | GRCh37 |
| NC_000019.8:g.7500488A>T | NCBI36 |
| NG_013374.1:g.451A>T | |
| NG_015806.1:g.11993A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.1249A>T MANE Select | ENSP00000264079.5:p.Thr417Ser | |
| ENST00000264079.10:c.1249A>T | ENSP00000264079.5:p.Thr417Ser | |
| ENST00000394321.9:n.1564A>T | ||
| ENST00000594692.1:n.245A>T | ||
| ENST00000595860.5:n.432A>T | ||
| ENST00000599334.1:c.126A>T | ||
| NM_020533.2:c.1249A>T | NP_065394.1:p.Thr417Ser | |
| NM_020533.3:c.1249A>T MANE Select | NP_065394.1:p.Thr417Ser |