Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.72007454G>A , CM000672.2:g.72007454G>A | GRCh38 |
| NC_000010.10:g.73767212G>A , CM000672.1:g.73767212G>A | GRCh37 |
| NC_000010.9:g.73437218G>A | NCBI36 |
| NG_012635.1:g.48093G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004273.5:c.423G>A MANE Select | NP_004264.2:p.Thr141= |
| ENST00000373115.5:c.423G>A MANE Select | ENSP00000362207.4:p.Thr141= |
| NM_004273.4:c.423G>A | NP_004264.2:p.Thr141= |
| ENST00000373115.4:c.423G>A | ENSP00000362207.4:p.Thr141= |
| XM_006718075.2:c.423G>A | XP_006718138.1:p.Thr141= |
| XM_006718075.4:c.423G>A | XP_006718138.1:p.Thr141= |
| XM_011540369.1:c.423G>A | XP_011538671.1:p.Thr141= |
| XM_011540369.2:c.423G>A | XP_011538671.1:p.Thr141= |