Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.78781863G>A , CM000667.2:g.78781863G>A | GRCh38 |
| NC_000005.9:g.78077686G>A , CM000667.1:g.78077686G>A | GRCh37 |
| NC_000005.8:g.78113442G>A | NCBI36 |
| NG_007089.1:g.209672C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264914.10:c.1325C>T MANE Select | ENSP00000264914.4:p.Thr442Met | |
| ENST00000264914.8:c.1325C>T | ENSP00000264914.4:p.Thr442Met | |
| ENST00000521011.1:n.290C>T | ||
| NM_000046.3:c.1325C>T | NP_000037.2:p.Thr442Met | |
| XM_011543390.1:c.1325C>T | XP_011541692.1:p.Thr442Met | |
| NM_000046.4:c.1325C>T | NP_000037.2:p.Thr442Met | |
| NM_000046.5:c.1325C>T MANE Select | NP_000037.2:p.Thr442Met |