Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6110494T= , CM000682.2:g.6110494T= | GRCh38 |
| NC_000020.10:g.6091141T= , CM000682.1:g.6091141T= | GRCh37 |
| NC_000020.9:g.6039141T= | NCBI36 |
| NG_016213.1:g.18051A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017671.5:c.550A= MANE Select | NP_060141.3:p.Ser184= |
| ENST00000217289.9:c.550A= MANE Select | ENSP00000217289.4:p.Ser184= |
| NM_017671.4:c.550A= | NP_060141.3:p.Ser184= |
| ENST00000217289.8:c.550A= | ENSP00000217289.4:p.Ser184= |
| ENST00000536936.1:c.-26+1983A= | ENSP00000441063.1:n.-26+1983A= |
| ENST00000699095.1:c.550A= | ENSP00000514127.1:p.Ser184= |
| ENST00000699096.1:n.1012A= | |
| ENST00000699098.1:c.550A= | ENSP00000514312.1:p.Ser184= |
| XM_024451935.1:c.550A= | XP_024307703.1:p.Ser184= |