Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171636128T= , CM000663.2:g.171636128T= | GRCh38 |
| NC_000001.10:g.171605268T= , CM000663.1:g.171605268T= | GRCh37 |
| NC_000001.9:g.169871891T= | NCBI36 |
| NG_008859.1:g.21506A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.1312A= (MYOC) MANE Select | ENSP00000037502.5:p.Thr438= | |
| ENST00000637303.1:c.235-2502T= (MYOCOS) | ENSP00000490048.1:n.235-2502T= | |
| ENST00000638471.1:c.*650A= (MYOC) | ENSP00000491206.1:n.*650A= | |
| ENST00000037502.10:c.1312A= (MYOC) | ENSP00000037502.5:p.Thr438= | |
| ENST00000614688.1:c.*276A= (MYOC) | ENSP00000478680.1:n.*276A= | |
| NM_000261.1:c.1312A= (MYOC) | NP_000252.1:p.Thr438= | |
| NM_000261.2:c.1312A= (MYOC) MANE Select | NP_000252.1:p.Thr438= |