Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47881741A= , CM000681.2:g.47881741A= | GRCh38 |
| NC_000019.9:g.48384998A= , CM000681.1:g.48384998A= | GRCh37 |
| NC_000019.8:g.53076810A= | NCBI36 |
| NG_016745.1:g.9657T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222002.4:c.472+343T= MANE Select | ENSP00000222002.2:n.472+343T= | |
| ENST00000222002.3:c.472+343T= | ENSP00000222002.2:n.472+343T= | |
| NM_003167.3:c.472+343T= | NP_003158.2:n.472+343T= | |
| NM_003167.4:c.472+343T= MANE Select | NP_003158.2:n.472+343T= |