Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75135062A= , CM000676.2:g.75135062A= | GRCh38 |
| NC_000014.8:g.75601765A= , CM000676.1:g.75601765A= | GRCh37 |
| NC_000014.7:g.74671518A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303575.9:c.539-56T= MANE Select | ENSP00000303145.4:n.539-56T= | |
| ENST00000303575.8:c.539-56T= | ENSP00000303145.4:n.539-56T= | |
| ENST00000555036.1:n.322-56T= | ||
| ENST00000555873.1:c.*175-56T= | ENSP00000450726.1:n.*175-56T= | |
| ENST00000556969.5:n.246-56T= | ||
| ENST00000557670.5:n.267-56T= | ||
| NM_006827.5:c.539-56T= | NP_006818.3:n.539-56T= | |
| NM_006827.6:c.539-56T= MANE Select | NP_006818.3:n.539-56T= |