HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171636202A>G , CM000663.2:g.171636202A>G | GRCh38 |
NC_000001.10:g.171605342A>G , CM000663.1:g.171605342A>G | GRCh37 |
NC_000001.9:g.169871965A>G | NCBI36 |
NG_008859.1:g.21432T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.1238T>C (MYOC) MANE Select | ENSP00000037502.5:p.Leu413Pro | |
ENST00000637303.1:c.235-2428A>G (MYOCOS) | ENSP00000490048.1:n.235-2428A>G | |
ENST00000638471.1:c.*576T>C (MYOC) | ENSP00000491206.1:n.*576T>C | |
ENST00000037502.10:c.1238T>C (MYOC) | ENSP00000037502.5:p.Leu413Pro | |
ENST00000614688.1:c.*202T>C (MYOC) | ENSP00000478680.1:n.*202T>C | |
NM_000261.1:c.1238T>C (MYOC) | NP_000252.1:p.Leu413Pro | |
NM_000261.2:c.1238T>C (MYOC) MANE Select | NP_000252.1:p.Leu413Pro |