Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52519829T= , CM000674.2:g.52519829T= | GRCh38 |
| NC_000012.11:g.52913613T= , CM000674.1:g.52913613T= | GRCh37 |
| NC_000012.10:g.51199880T= | NCBI36 |
| NG_008297.1:g.5631A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.468A= MANE Select | ENSP00000252242.4:p.Gln156= | |
| ENST00000252242.8:c.468A= | ENSP00000252242.4:p.Gln156= | |
| ENST00000549420.1:c.138A= | ENSP00000447209.1:p.Gln46= | |
| ENST00000551275.1:c.363A= | ENSP00000448041.1:p.Gln121= | |
| ENST00000552629.5:n.566A= | ||
| NM_000424.3:c.468A= | NP_000415.2:p.Gln156= | |
| NM_000424.4:c.468A= MANE Select | NP_000415.2:p.Gln156= |