Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454549A= , CM000679.2:g.7454549A= | GRCh38 |
| NC_000017.10:g.7357868A= , CM000679.1:g.7357868A= | GRCh37 |
| NC_000017.9:g.7298592A= | NCBI36 |
| NG_008026.1:g.14463A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.1044+29A= MANE Select | ENSP00000304290.2:n.1044+29A= | |
| ENST00000306071.6:c.1044+29A= | ENSP00000304290.2:n.1044+29A= | |
| ENST00000536404.6:c.828+29A= | ENSP00000439209.2:n.828+29A= | |
| ENST00000570557.5:c.707+29A= | ||
| ENST00000573209.1:n.1988+29A= | ||
| ENST00000576360.1:c.681+29A= | ENSP00000459092.1:n.681+29A= | |
| NM_000747.2:c.1044+29A= | NP_000738.2:n.1044+29A= | |
| NM_000747.3:c.1044+29A= MANE Select | NP_000738.2:n.1044+29A= |