Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23418010T>A , CM000676.2:g.23418010T>A | GRCh38 |
| NC_000014.8:g.23887219T>A , CM000676.1:g.23887219T>A | GRCh37 |
| NC_000014.7:g.22957059T>A | NCBI36 |
| NG_007884.1:g.22652A>T , LRG_384:g.22652A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000257.4:c.4169+200A>T (MYH7) MANE Select | NP_000248.2:n.4169+200A>T |
| ENST00000355349.4:c.4169+200A>T (MYH7) MANE Select | ENSP00000347507.3:n.4169+200A>T |
| NM_000257.3:c.4169+200A>T (MYH7) | NP_000248.2:n.4169+200A>T |
| NR_030624.1:n.54A>T (MIR208B) | |
| ENST00000355349.3:c.4169+200A>T (MYH7) | ENSP00000347507.3:n.4169+200A>T |
| XM_017021340.1:c.4169+200A>T (MYH7) | XP_016876829.1:n.4169+200A>T |