Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.22123994C= , CM000663.2:g.22123994C= | GRCh38 |
| NC_000001.10:g.22450487C= , CM000663.1:g.22450487C= | GRCh37 |
| NC_000001.9:g.22323074C= | NCBI36 |
| NG_008974.1:g.24033G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290167.11:c.314-2418G= MANE Select | ENSP00000290167.5:n.314-2418G= | |
| ENST00000290167.10:c.314-2418G= | ENSP00000290167.5:n.314-2418G= | |
| NM_030761.4:c.314-2418G= | NP_110388.2:n.314-2418G= | |
| XM_011541597.1:c.380-2418G= | XP_011539899.1:n.380-2418G= | |
| XM_011541598.1:c.149-2418G= | XP_011539900.1:n.149-2418G= | |
| XM_011541597.2:c.380-2418G= | XP_011539899.1:n.380-2418G= | |
| XM_011541598.2:c.149-2418G= | XP_011539900.1:n.149-2418G= | |
| NM_030761.5:c.314-2418G= MANE Select | NP_110388.2:n.314-2418G= |