Linked Data
ClinVar Variation Id:
7960
dbSNP Id:
rs74315341
gnomAD v4:
1-171636686-C-T
ERepo:
CA119185/MONDO:0020367/019
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171636686C>T , CM000663.2:g.171636686C>T | GRCh38 |
| NC_000001.10:g.171605826C>T , CM000663.1:g.171605826C>T | GRCh37 |
| NC_000001.9:g.169872449C>T | NCBI36 |
| NG_008859.1:g.20948G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000037502.11:c.754G>A (MYOC) MANE Select | ENSP00000037502.5:p.Gly252Arg | |
| ENST00000637303.1:c.235-1944C>T (MYOCOS) | ENSP00000490048.1:n.235-1944C>T | |
| ENST00000638471.1:c.*92G>A (MYOC) | ENSP00000491206.1:n.*92G>A | |
| ENST00000037502.10:c.754G>A (MYOC) | ENSP00000037502.5:p.Gly252Arg | |
| ENST00000614688.1:c.754G>A (MYOC) | ENSP00000478680.1:p.Gly252Arg | |
| NM_000261.1:c.754G>A (MYOC) | NP_000252.1:p.Gly252Arg | |
| NM_000261.2:c.754G>A (MYOC) MANE Select | NP_000252.1:p.Gly252Arg |