Linked Data
dbSNP Id:
rs2102944314
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171635679G>A , CM000663.2:g.171635679G>A | GRCh38 |
| NC_000001.10:g.171604819G>A , CM000663.1:g.171604819G>A | GRCh37 |
| NC_000001.9:g.169871442G>A | NCBI36 |
| NG_008859.1:g.21955C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.*246C>T (MYOC) MANE Select | ENSP00000037502.5:n.*246C>T | |
| ENST00000637303.1:c.235-2951G>A (MYOCOS) | ENSP00000490048.1:n.235-2951G>A | |
| ENST00000638471.1:c.*1099C>T (MYOC) | ENSP00000491206.1:n.*1099C>T | |
| ENST00000037502.10:c.*246C>T (MYOC) | ENSP00000037502.5:n.*246C>T | |
| ENST00000614688.1:c.*725C>T (MYOC) | ENSP00000478680.1:n.*725C>T | |
| NM_000261.1:c.*246C>T (MYOC) | NP_000252.1:n.*246C>T | |
| NM_000261.2:c.*246C>T (MYOC) MANE Select | NP_000252.1:n.*246C>T |