Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48875911A>T , CM000681.2:g.48875911A>T | GRCh38 |
| NC_000019.9:g.49379168A>T , CM000681.1:g.49379168A>T | GRCh37 |
| NC_000019.8:g.54070980A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000600406.2:c.*818A>T | ENSP00000469239.2:n.*818A>T | |
| ENST00000704026.1:c.1678A>T | ENSP00000515636.1:p.Thr560Ser | |
| ENST00000704027.1:c.2011A>T | ENSP00000515637.1:p.Thr671Ser | |
| ENST00000200453.6:c.1963A>T MANE Select | ENSP00000200453.4:p.Thr655Ser | |
| ENST00000200453.5:c.1963A>T | ENSP00000200453.4:p.Thr655Ser | |
| ENST00000600406.1:c.1594A>T | ||
| NM_014330.3:c.1963A>T | NP_055145.3:p.Thr655Ser | |
| NM_014330.5:c.1963A>T MANE Select | NP_055145.3:p.Thr655Ser |