Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171635734A= , CM000663.2:g.171635734A= | GRCh38 |
| NC_000001.10:g.171604874A= , CM000663.1:g.171604874A= | GRCh37 |
| NC_000001.9:g.169871497A= | NCBI36 |
| NG_008859.1:g.21900T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.*191T= (MYOC) MANE Select | ENSP00000037502.5:n.*191T= | |
| ENST00000637303.1:c.235-2896A= (MYOCOS) | ENSP00000490048.1:n.235-2896A= | |
| ENST00000638471.1:c.*1044T= (MYOC) | ENSP00000491206.1:n.*1044T= | |
| ENST00000037502.10:c.*191T= (MYOC) | ENSP00000037502.5:n.*191T= | |
| ENST00000614688.1:c.*670T= (MYOC) | ENSP00000478680.1:n.*670T= | |
| NM_000261.1:c.*191T= (MYOC) | NP_000252.1:n.*191T= | |
| NM_000261.2:c.*191T= (MYOC) MANE Select | NP_000252.1:n.*191T= |