Linked Data
ClinVar Variation Id:
293707
dbSNP Id:
rs886045564
gnomAD v2:
1-171604994-C-T
gnomAD v3:
1-171635854-C-T
gnomAD v4:
1-171635854-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171635854C>T , CM000663.2:g.171635854C>T | GRCh38 |
| NC_000001.10:g.171604994C>T , CM000663.1:g.171604994C>T | GRCh37 |
| NC_000001.9:g.169871617C>T | NCBI36 |
| NG_008859.1:g.21780G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.*71G>A (MYOC) MANE Select | ENSP00000037502.5:n.*71G>A | |
| ENST00000637303.1:c.235-2776C>T (MYOCOS) | ENSP00000490048.1:n.235-2776C>T | |
| ENST00000638471.1:c.*924G>A (MYOC) | ENSP00000491206.1:n.*924G>A | |
| ENST00000037502.10:c.*71G>A (MYOC) | ENSP00000037502.5:n.*71G>A | |
| ENST00000614688.1:c.*550G>A (MYOC) | ENSP00000478680.1:n.*550G>A | |
| NM_000261.1:c.*71G>A (MYOC) | NP_000252.1:n.*71G>A | |
| NM_000261.2:c.*71G>A (MYOC) MANE Select | NP_000252.1:n.*71G>A |