Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171635954T>G , CM000663.2:g.171635954T>G | GRCh38 |
| NC_000001.10:g.171605094T>G , CM000663.1:g.171605094T>G | GRCh37 |
| NC_000001.9:g.169871717T>G | NCBI36 |
| NG_008859.1:g.21680A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000261.2:c.1486A>C (MYOC) MANE Select | NP_000252.1:p.Thr496Pro |
| ENST00000037502.11:c.1486A>C (MYOC) MANE Select | ENSP00000037502.5:p.Thr496Pro |
| NM_000261.1:c.1486A>C (MYOC) | NP_000252.1:p.Thr496Pro |
| ENST00000037502.10:c.1486A>C (MYOC) | ENSP00000037502.5:p.Thr496Pro |
| ENST00000614688.1:c.*450A>C (MYOC) | ENSP00000478680.1:n.*450A>C |
| ENST00000637303.1:c.235-2676T>G (MYOCOS) | ENSP00000490048.1:n.235-2676T>G |
| ENST00000638471.1:c.*824A>C (MYOC) | ENSP00000491206.1:n.*824A>C |