Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10420361C>G , CM000679.2:g.10420361C>G | GRCh38 |
| NC_000017.10:g.10323678C>G , CM000679.1:g.10323678C>G | GRCh37 |
| NC_000017.9:g.10264403C>G | NCBI36 |
| NG_013015.1:g.6590G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403437.2:c.-30-104G>C (MYH8) MANE Select | ENSP00000384330.2:n.-30-104G>C | |
| NM_002472.2:c.-30-104G>C (MYH8) | NP_002463.2:n.-30-104G>C | |
| NR_125367.1:n.167+14123C>G (MYHAS) | ||
| XM_011523873.1:c.-30-104G>C (MYH8) | XP_011522175.1:n.-30-104G>C | |
| XM_011523874.1:c.-26-108G>C (MYH8) | XP_011522176.1:n.-26-108G>C | |
| NM_002472.3:c.-30-104G>C (MYH8) MANE Select | NP_002463.2:n.-30-104G>C |