HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23416314_23416315insC , CM000676.2:g.23416314_23416315insC | GRCh38 |
NC_000014.8:g.23885523_23885524insC , CM000676.1:g.23885523_23885524insC | GRCh37 |
NC_000014.7:g.22955363_22955364insC | NCBI36 |
NG_007884.1:g.24347_24348insG , LRG_384:g.24347_24348insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.4645-3_4645-2insG (MYH7) MANE Select | ENSP00000347507.3:n.4645-3_4645-2insG | |
ENST00000355349.3:c.4645-3_4645-2insG (MYH7) | ENSP00000347507.3:n.4645-3_4645-2insG | |
NM_000257.3:c.4645-3_4645-2insG (MYH7) | NP_000248.2:n.4645-3_4645-2insG | |
NR_126491.1:n.558+17_558+18insC (MHRT) | ||
XM_017021340.1:c.4645-3_4645-2insG (MYH7) | XP_016876829.1:n.4645-3_4645-2insG | |
NM_000257.4:c.4645-3_4645-2insG (MYH7) MANE Select | NP_000248.2:n.4645-3_4645-2insG |