Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137199874T>A , CM000671.2:g.137199874T>A | GRCh38 |
| NC_000009.11:g.140094326T>A , CM000671.1:g.140094326T>A | GRCh37 |
| NC_000009.10:g.139214147T>A | NCBI36 |
| NG_027801.1:g.5838A>T | |
| NG_027801.2:g.9320A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001128228.3:c.838A>T MANE Select | NP_001121700.2:p.Thr280Ser |
| ENST00000409012.6:c.838A>T MANE Select | ENSP00000387100.4:p.Thr280Ser |
| NM_001128228.2:c.838A>T | NP_001121700.2:p.Thr280Ser |
| ENST00000333046.8:c.232A>T | ENSP00000327617.4:p.Thr78Ser |
| ENST00000409012.4:c.838A>T | ENSP00000387100.4:p.Thr280Ser |
| ENST00000541945.1:n.90+4230A>T |