Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129813771C= , CM000671.2:g.129813771C= | GRCh38 |
| NC_000009.11:g.132576050C= , CM000671.1:g.132576050C= | GRCh37 |
| NC_000009.10:g.131615871C= | NCBI36 |
| NG_008049.1:g.15392G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.*201G= MANE Select | ENSP00000345719.4:n.*201G= | |
| ENST00000651202.1:c.*468G= | ENSP00000498222.1:n.*468G= | |
| ENST00000351698.4:c.*201G= | ENSP00000345719.4:n.*201G= | |
| ENST00000474192.1:n.784G= | ||
| NM_000113.2:c.*201G= | NP_000104.1:n.*201G= | |
| XR_929731.3:n.1395G= | ||
| NM_000113.3:c.*201G= MANE Select | NP_000104.1:n.*201G= |