Linked Data
ClinVar Variation Id:
1686783
ClinVar RCV Id:
RCV002248288
dbSNP Id:
rs754237376
ExAC:
1:171605301 C / T
gnomAD v2:
1-171605301-C-T
gnomAD v3:
1-171636161-C-T
gnomAD v4:
1-171636161-C-T
COSMIC:
COSM1216468
ERepo:
CA1244050/MONDO:0007665/019
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171636161C>T , CM000663.2:g.171636161C>T | GRCh38 |
| NC_000001.10:g.171605301C>T , CM000663.1:g.171605301C>T | GRCh37 |
| NC_000001.9:g.169871924C>T | NCBI36 |
| NG_008859.1:g.21473G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.1279G>A (MYOC) MANE Select | ENSP00000037502.5:p.Ala427Thr | |
| ENST00000637303.1:c.235-2469C>T (MYOCOS) | ENSP00000490048.1:n.235-2469C>T | |
| ENST00000638471.1:c.*617G>A (MYOC) | ENSP00000491206.1:n.*617G>A | |
| ENST00000037502.10:c.1279G>A (MYOC) | ENSP00000037502.5:p.Ala427Thr | |
| ENST00000614688.1:c.*243G>A (MYOC) | ENSP00000478680.1:n.*243G>A | |
| NM_000261.1:c.1279G>A (MYOC) | NP_000252.1:p.Ala427Thr | |
| NM_000261.2:c.1279G>A (MYOC) MANE Select | NP_000252.1:p.Ala427Thr |