Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.144474610G>A , CM000670.2:g.144474610G>A | GRCh38 |
| NC_000008.10:g.145699993G>A , CM000670.1:g.145699993G>A | GRCh37 |
| NC_000008.9:g.145670801G>A | NCBI36 |
| NG_030003.1:g.6726C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003923.3:c.726C>T MANE Select | NP_003914.1:p.Thr242= |
| ENST00000377317.5:c.726C>T MANE Select | ENSP00000366534.4:p.Thr242= |
| NM_003923.2:c.726C>T | NP_003914.1:p.Thr242= |
| ENST00000377317.4:c.726C>T | ENSP00000366534.4:p.Thr242= |