Linked Data
gnomAD v4:
1-171635675-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171635675C>A , CM000663.2:g.171635675C>A | GRCh38 |
| NC_000001.10:g.171604815C>A , CM000663.1:g.171604815C>A | GRCh37 |
| NC_000001.9:g.169871438C>A | NCBI36 |
| NG_008859.1:g.21959G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.*250G>T (MYOC) MANE Select | ENSP00000037502.5:n.*250G>T | |
| ENST00000637303.1:c.235-2955C>A (MYOCOS) | ENSP00000490048.1:n.235-2955C>A | |
| ENST00000638471.1:c.*1103G>T (MYOC) | ENSP00000491206.1:n.*1103G>T | |
| ENST00000037502.10:c.*250G>T (MYOC) | ENSP00000037502.5:n.*250G>T | |
| ENST00000614688.1:c.*729G>T (MYOC) | ENSP00000478680.1:n.*729G>T | |
| NM_000261.1:c.*250G>T (MYOC) | NP_000252.1:n.*250G>T | |
| NM_000261.2:c.*250G>T (MYOC) MANE Select | NP_000252.1:n.*250G>T |