Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171635624A>G , CM000663.2:g.171635624A>G | GRCh38 |
| NC_000001.10:g.171604764A>G , CM000663.1:g.171604764A>G | GRCh37 |
| NC_000001.9:g.169871387A>G | NCBI36 |
| NG_008859.1:g.22010T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.*301T>C (MYOC) MANE Select | ENSP00000037502.5:n.*301T>C | |
| ENST00000637303.1:c.235-3006A>G (MYOCOS) | ENSP00000490048.1:n.235-3006A>G | |
| ENST00000638471.1:c.*1154T>C (MYOC) | ENSP00000491206.1:n.*1154T>C | |
| ENST00000037502.10:c.*301T>C (MYOC) | ENSP00000037502.5:n.*301T>C | |
| ENST00000614688.1:c.*780T>C (MYOC) | ENSP00000478680.1:n.*780T>C | |
| NM_000261.1:c.*301T>C (MYOC) | NP_000252.1:n.*301T>C | |
| NM_000261.2:c.*301T>C (MYOC) MANE Select | NP_000252.1:n.*301T>C |