Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138945579A= , CM000665.2:g.138945579A= | GRCh38 |
| NC_000003.11:g.138664421A= , CM000665.1:g.138664421A= | GRCh37 |
| NC_000003.10:g.140147111A= | NCBI36 |
| NG_012454.1:g.6562T= | |
| NG_029796.1:g.3346A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.*13T= MANE Select | ENSP00000497217.1:n.*13T= | |
| ENST00000330315.3:c.*13T= | ENSP00000333188.3:n.*13T= | |
| NM_023067.3:c.*13T= | NP_075555.1:n.*13T= | |
| NM_023067.4:c.*13T= MANE Select | NP_075555.1:n.*13T= |