HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23416330_23416342del , CM000676.2:g.23416330_23416342del | GRCh38 |
NC_000014.8:g.23885539_23885551del , CM000676.1:g.23885539_23885551del | GRCh37 |
NC_000014.7:g.22955379_22955391del | NCBI36 |
NG_007884.1:g.24322_24334del , LRG_384:g.24322_24334del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.4645-28_4645-16del (MYH7) MANE Select | ENSP00000347507.3:n.4645-28_4645-16del | |
ENST00000355349.3:c.4645-28_4645-16del (MYH7) | ENSP00000347507.3:n.4645-28_4645-16del | |
NM_000257.3:c.4645-28_4645-16del (MYH7) | NP_000248.2:n.4645-28_4645-16del | |
NR_126491.1:n.558+33_558+45del (MHRT) | ||
XM_017021340.1:c.4645-28_4645-16del (MYH7) | XP_016876829.1:n.4645-28_4645-16del | |
NM_000257.4:c.4645-28_4645-16del (MYH7) MANE Select | NP_000248.2:n.4645-28_4645-16del |