Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64753568C>T , CM000673.2:g.64753568C>T | GRCh38 |
| NC_000011.9:g.64521040C>T , CM000673.1:g.64521040C>T | GRCh37 |
| NC_000011.8:g.64277616C>T | NCBI36 |
| NG_013018.1:g.12148G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005609.4:c.1354G>A MANE Select | NP_005600.1:p.Ala452Thr |
| ENST00000164139.4:c.1354G>A MANE Select | ENSP00000164139.3:p.Ala452Thr |
| NM_001164716.1:c.1090G>A | NP_001158188.1:p.Ala364Thr |
| NM_005609.2:c.1354G>A | NP_005600.1:p.Ala452Thr |
| NM_005609.3:c.1354G>A | NP_005600.1:p.Ala452Thr |
| ENST00000164139.3:c.1354G>A | ENSP00000164139.3:p.Ala452Thr |
| ENST00000377432.7:c.1090G>A | ENSP00000366650.3:p.Ala364Thr |