Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.43337834A= , CM000663.2:g.43337834A= | GRCh38 |
| NC_000001.10:g.43803505A= , CM000663.1:g.43803505A= | GRCh37 |
| NC_000001.9:g.43576092A= | NCBI36 |
| NG_007525.1:g.5031A= , LRG_510:g.5031A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372470.9:c.-15A= MANE Select | ENSP00000361548.3:n.-15A= | |
| ENST00000372470.7:c.-15A= | ENSP00000361548.3:n.-15A= | |
| NM_005373.2:c.-15A= , LRG_510t1:c.-15A= | NP_005364.1:n.-15A= | |
| XM_011541478.1:c.-15A= | XP_011539780.1:n.-15A= | |
| XM_017001320.1:c.-15A= | XP_016856809.1:n.-15A= | |
| NM_005373.3:c.-15A= MANE Select | NP_005364.1:n.-15A= |