Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.78565554T= , CM000677.2:g.78565554T= | GRCh38 |
| NC_000015.9:g.78857896T= , CM000677.1:g.78857896T= | GRCh37 |
| NC_000015.8:g.76644951T= | NCBI36 |
| NG_023328.1:g.5035T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000745.4:c.-166T= MANE Select | NP_000736.2:n.-166T= |
| ENST00000299565.9:c.-166T= MANE Select | ENSP00000299565.5:n.-166T= |
| NM_000745.3:c.-166T= | NP_000736.2:n.-166T= |
| NM_001307945.1:c.-166T= | NP_001294874.1:n.-166T= |
| NM_001307945.2:c.-166T= | NP_001294874.1:n.-166T= |
| NM_001395171.1:c.-166T= | NP_001382100.1:n.-166T= |
| NM_001395172.1:c.-166T= | NP_001382101.1:n.-166T= |
| NM_001395173.1:c.-166T= | NP_001382102.1:n.-166T= |
| NM_001395174.1:c.-166T= | NP_001382103.1:n.-166T= |
| NM_001395175.1:c.-166T= | NP_001382104.1:n.-166T= |
| XM_005254142.2:c.-166T= | XP_005254199.1:n.-166T= |