Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171636464C>T , CM000663.2:g.171636464C>T | GRCh38 |
| NC_000001.10:g.171605604C>T , CM000663.1:g.171605604C>T | GRCh37 |
| NC_000001.9:g.169872227C>T | NCBI36 |
| NG_008859.1:g.21170G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000261.2:c.976G>A (MYOC) MANE Select | NP_000252.1:p.Gly326Ser |
| ENST00000037502.11:c.976G>A (MYOC) MANE Select | ENSP00000037502.5:p.Gly326Ser |
| NM_000261.1:c.976G>A (MYOC) | NP_000252.1:p.Gly326Ser |
| ENST00000037502.10:c.976G>A (MYOC) | ENSP00000037502.5:p.Gly326Ser |
| ENST00000614688.1:c.976G>A (MYOC) | ENSP00000478680.1:p.Gly326Ser |
| ENST00000637303.1:c.235-2166C>T (MYOCOS) | ENSP00000490048.1:n.235-2166C>T |
| ENST00000638471.1:c.*314G>A (MYOC) | ENSP00000491206.1:n.*314G>A |