Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.80744561C>G , CM000667.2:g.80744561C>G | GRCh38 |
| NC_000005.9:g.80040380C>G , CM000667.1:g.80040380C>G | GRCh37 |
| NC_000005.8:g.80076136C>G | NCBI36 |
| NG_016607.1:g.95087C>G | |
| NG_016607.2:g.95087C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002439.5:c.1709C>G MANE Select | NP_002430.3:p.Ser570Ter |
| ENST00000265081.7:c.1709C>G MANE Select | ENSP00000265081.6:p.Ser570Ter |
| NM_002439.4:c.1709C>G | NP_002430.3:p.Ser570Ter |
| ENST00000265081.6:c.1709C>G | ENSP00000265081.6:p.Ser570Ter |
| ENST00000512258.1:n.558C>G | |
| ENST00000658259.1:c.1541C>G | ENSP00000499617.1:p.Ser514Ter |
| ENST00000667069.1:c.1568+15596C>G | ENSP00000499502.1:n.1568+15596C>G |
| ENST00000670357.1:c.1709C>G | ENSP00000499791.1:p.Ser570Ter |