Linked Data
ClinVar Variation Id:
2505292
ClinVar RCV Id:
RCV003233469
dbSNP Id:
rs369169139
gnomAD v2:
1-171605701-C-T
gnomAD v3:
1-171636561-C-T
gnomAD v4:
1-171636561-C-T
COSMIC:
COSM3478333
ERepo:
CA32686049/MONDO:0007665/019
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171636561C>T , CM000663.2:g.171636561C>T | GRCh38 |
| NC_000001.10:g.171605701C>T , CM000663.1:g.171605701C>T | GRCh37 |
| NC_000001.9:g.169872324C>T | NCBI36 |
| NG_008859.1:g.21073G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.879G>A (MYOC) MANE Select | ENSP00000037502.5:p.Thr293= | |
| ENST00000637303.1:c.235-2069C>T (MYOCOS) | ENSP00000490048.1:n.235-2069C>T | |
| ENST00000638471.1:c.*217G>A (MYOC) | ENSP00000491206.1:n.*217G>A | |
| ENST00000037502.10:c.879G>A (MYOC) | ENSP00000037502.5:p.Thr293= | |
| ENST00000614688.1:c.879G>A (MYOC) | ENSP00000478680.1:p.Thr293= | |
| NM_000261.1:c.879G>A (MYOC) | NP_000252.1:p.Thr293= | |
| NM_000261.2:c.879G>A (MYOC) MANE Select | NP_000252.1:p.Thr293= |