Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075709T>A , CM000679.2:g.8075709T>A | GRCh38 |
| NC_000017.10:g.7979027T>A , CM000679.1:g.7979027T>A | GRCh37 |
| NC_000017.9:g.7919752T>A | NCBI36 |
| NG_007099.1:g.16995A>T | |
| NG_007099.2:g.17008A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1540A>T MANE Select | ENSP00000497784.1:p.Thr514Ser | |
| ENST00000649809.1:c.604A>T | ENSP00000496845.1:p.Thr202Ser | |
| ENST00000319144.4:c.1540A>T | ENSP00000315167.4:p.Thr514Ser | |
| ENST00000577351.5:n.479+466A>T | ||
| NM_001139.2:c.1540A>T | NP_001130.1:p.Thr514Ser | |
| NM_001139.3:c.1540A>T MANE Select | NP_001130.1:p.Thr514Ser |