HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171636641A>C , CM000663.2:g.171636641A>C | GRCh38 |
NC_000001.10:g.171605781A>C , CM000663.1:g.171605781A>C | GRCh37 |
NC_000001.9:g.169872404A>C | NCBI36 |
NG_008859.1:g.20993T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.799T>G (MYOC) MANE Select | ENSP00000037502.5:p.Tyr267Asp | |
ENST00000637303.1:c.235-1989A>C (MYOCOS) | ENSP00000490048.1:n.235-1989A>C | |
ENST00000638471.1:c.*137T>G (MYOC) | ENSP00000491206.1:n.*137T>G | |
ENST00000037502.10:c.799T>G (MYOC) | ENSP00000037502.5:p.Tyr267Asp | |
ENST00000614688.1:c.799T>G (MYOC) | ENSP00000478680.1:p.Tyr267Asp | |
NM_000261.1:c.799T>G (MYOC) | NP_000252.1:p.Tyr267Asp | |
NM_000261.2:c.799T>G (MYOC) MANE Select | NP_000252.1:p.Tyr267Asp |