Linked Data
dbSNP Id:
rs1652899808
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171635612T>A , CM000663.2:g.171635612T>A | GRCh38 |
| NC_000001.10:g.171604752T>A , CM000663.1:g.171604752T>A | GRCh37 |
| NC_000001.9:g.169871375T>A | NCBI36 |
| NG_008859.1:g.22022A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.*313A>T (MYOC) MANE Select | ENSP00000037502.5:n.*313A>T | |
| ENST00000637303.1:c.235-3018T>A (MYOCOS) | ENSP00000490048.1:n.235-3018T>A | |
| ENST00000638471.1:c.*1166A>T (MYOC) | ENSP00000491206.1:n.*1166A>T | |
| ENST00000037502.10:c.*313A>T (MYOC) | ENSP00000037502.5:n.*313A>T | |
| ENST00000614688.1:c.*792A>T (MYOC) | ENSP00000478680.1:n.*792A>T | |
| NM_000261.1:c.*313A>T (MYOC) | NP_000252.1:n.*313A>T | |
| NM_000261.2:c.*313A>T (MYOC) MANE Select | NP_000252.1:n.*313A>T |