Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2432453G>A , CM000681.2:g.2432453G>A | GRCh38 |
| NC_000019.9:g.2432451G>A , CM000681.1:g.2432451G>A | GRCh37 |
| NC_000019.8:g.2383451G>A | NCBI36 |
| NG_008355.1:g.29508C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032737.4:c.1553C>T MANE Select | NP_116126.3:p.Thr518Met |
| ENST00000325327.4:c.1553C>T MANE Select | ENSP00000327054.3:p.Thr518Met |
| NM_032737.3:c.1553C>T | NP_116126.3:p.Thr518Met |
| ENST00000325327.3:c.1553C>T | ENSP00000327054.3:p.Thr518Met |
| ENST00000532465.1:n.145C>T | |
| XM_011528378.1:c.1553C>T | XP_011526680.1:p.Thr518Met |
| XM_011528379.1:c.1205C>T | XP_011526681.1:p.Thr402Met |