Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4934489T>A , CM000679.2:g.4934489T>A | GRCh38 |
| NC_000017.10:g.4837784T>A , CM000679.1:g.4837784T>A | GRCh37 |
| NC_000017.9:g.4778525T>A | NCBI36 |
| NG_008767.2:g.7195T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000173.7:c.1885T>A MANE Select | NP_000164.5:p.Ser629Thr |
| ENST00000329125.6:c.1885T>A MANE Select | ENSP00000329380.5:p.Ser629Thr |
| NM_000173.6:c.1885T>A | NP_000164.5:p.Ser629Thr |
| ENST00000329125.5:c.1885T>A | ENSP00000329380.5:p.Ser629Thr |
| ENST00000611961.1:c.1807T>A | ENSP00000484439.1:p.Ser603Thr |