Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.312269A= , CM000674.2:g.312269A= | GRCh38 |
| NC_000012.11:g.421435A= , CM000674.1:g.421435A= | GRCh37 |
| NC_000012.10:g.291696A= | NCBI36 |
| NG_046993.1:g.82187T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399788.7:c.3036+787T= MANE Select | ENSP00000382688.2:n.3036+787T= | |
| ENST00000382815.8:c.3036+787T= | ENSP00000372265.5:n.3036+787T= | |
| ENST00000399788.6:c.3036+787T= | ENSP00000382688.2:n.3036+787T= | |
| ENST00000544760.1:c.1893+787T= | ENSP00000440622.1:n.1893+787T= | |
| NM_001042603.2:c.3036+787T= | NP_001036068.1:n.3036+787T= | |
| NM_001042603.3:c.3036+787T= MANE Select | NP_001036068.1:n.3036+787T= |