Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6089031A= , CM000682.2:g.6089031A= | GRCh38 |
| NC_000020.10:g.6069678A= , CM000682.1:g.6069678A= | GRCh37 |
| NC_000020.9:g.6017678A= | NCBI36 |
| NG_016213.1:g.39514T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017671.5:c.1198T= MANE Select | NP_060141.3:p.Ser400= |
| ENST00000217289.9:c.1198T= MANE Select | ENSP00000217289.4:p.Ser400= |
| NM_017671.4:c.1198T= | NP_060141.3:p.Ser400= |
| ENST00000217289.8:c.1198T= | ENSP00000217289.4:p.Ser400= |
| ENST00000478194.1:n.158T= | |
| ENST00000536936.1:c.427T= | ENSP00000441063.1:p.Ser143= |
| ENST00000699095.1:c.1198T= | ENSP00000514127.1:p.Ser400= |
| ENST00000699096.1:n.1660T= | |
| XM_024451935.1:c.1198T= | XP_024307703.1:p.Ser400= |