Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10404338C= , CM000679.2:g.10404338C= | GRCh38 |
| NC_000017.10:g.10307655C= , CM000679.1:g.10307655C= | GRCh37 |
| NC_000017.9:g.10248380C= | NCBI36 |
| NG_013015.1:g.22613G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002472.3:c.2680G= (MYH8) MANE Select | NP_002463.2:p.Val894= |
| ENST00000403437.2:c.2680G= (MYH8) MANE Select | ENSP00000384330.2:p.Val894= |
| NM_002472.2:c.2680G= (MYH8) | NP_002463.2:p.Val894= |
| NR_125367.1:n.77-1810C= (MYHAS) | |
| XM_011523873.1:c.2776G= (MYH8) | XP_011522175.1:p.Val926= |
| XM_011523874.1:c.2776G= (MYH8) | XP_011522176.1:p.Val926= |