Linked Data
ClinVar Variation Id:
1342207
ClinVar RCV Id:
RCV001838874
dbSNP Id:
rs554235897
ExAC:
1:171605168 T / C
gnomAD v2:
1-171605168-T-C
gnomAD v3:
1-171636028-T-C
gnomAD v4:
1-171636028-T-C
ERepo:
CA1244027/MONDO:0007665/019
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171636028T>C , CM000663.2:g.171636028T>C | GRCh38 |
| NC_000001.10:g.171605168T>C , CM000663.1:g.171605168T>C | GRCh37 |
| NC_000001.9:g.169871791T>C | NCBI36 |
| NG_008859.1:g.21606A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.1412A>G (MYOC) MANE Select | ENSP00000037502.5:p.Tyr471Cys | |
| ENST00000637303.1:c.235-2602T>C (MYOCOS) | ENSP00000490048.1:n.235-2602T>C | |
| ENST00000638471.1:c.*750A>G (MYOC) | ENSP00000491206.1:n.*750A>G | |
| ENST00000037502.10:c.1412A>G (MYOC) | ENSP00000037502.5:p.Tyr471Cys | |
| ENST00000614688.1:c.*376A>G (MYOC) | ENSP00000478680.1:n.*376A>G | |
| NM_000261.1:c.1412A>G (MYOC) | NP_000252.1:p.Tyr471Cys | |
| NM_000261.2:c.1412A>G (MYOC) MANE Select | NP_000252.1:p.Tyr471Cys |