Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10415357C>T , CM000679.2:g.10415357C>T | GRCh38 |
| NC_000017.10:g.10318674C>T , CM000679.1:g.10318674C>T | GRCh37 |
| NC_000017.9:g.10259399C>T | NCBI36 |
| NG_013015.1:g.11594G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002472.3:c.676G>A (MYH8) MANE Select | NP_002463.2:p.Ala226Thr |
| ENST00000403437.2:c.676G>A (MYH8) MANE Select | ENSP00000384330.2:p.Ala226Thr |
| NM_002472.2:c.676G>A (MYH8) | NP_002463.2:p.Ala226Thr |
| NR_125367.1:n.167+9119C>T (MYHAS) | |
| XM_011523873.1:c.676G>A (MYH8) | XP_011522175.1:p.Ala226Thr |
| XM_011523874.1:c.676G>A (MYH8) | XP_011522176.1:p.Ala226Thr |