Linked Data
gnomAD v4:
1-171635592-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171635592C>A , CM000663.2:g.171635592C>A | GRCh38 |
| NC_000001.10:g.171604732C>A , CM000663.1:g.171604732C>A | GRCh37 |
| NC_000001.9:g.169871355C>A | NCBI36 |
| NG_008859.1:g.22042G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.*333G>T (MYOC) MANE Select | ENSP00000037502.5:n.*333G>T | |
| ENST00000637303.1:c.235-3038C>A (MYOCOS) | ENSP00000490048.1:n.235-3038C>A | |
| ENST00000638471.1:c.*1186G>T (MYOC) | ENSP00000491206.1:n.*1186G>T | |
| ENST00000037502.10:c.*333G>T (MYOC) | ENSP00000037502.5:n.*333G>T | |
| ENST00000614688.1:c.*812G>T (MYOC) | ENSP00000478680.1:n.*812G>T | |
| NM_000261.1:c.*333G>T (MYOC) | NP_000252.1:n.*333G>T | |
| NM_000261.2:c.*333G>T (MYOC) MANE Select | NP_000252.1:n.*333G>T |