HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23415860_23415866del , CM000676.2:g.23415860_23415866del | GRCh38 |
NC_000014.8:g.23885069_23885075del , CM000676.1:g.23885069_23885075del | GRCh37 |
NC_000014.7:g.22954909_22954915del | NCBI36 |
NG_007884.1:g.24800_24806del , LRG_384:g.24800_24806del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.4954-30_4954-24del (MYH7) MANE Select | ENSP00000347507.3:n.4954-30_4954-24del | |
ENST00000355349.3:c.4954-30_4954-24del (MYH7) | ENSP00000347507.3:n.4954-30_4954-24del | |
NM_000257.3:c.4954-30_4954-24del (MYH7) | NP_000248.2:n.4954-30_4954-24del | |
NR_126491.1:n.261+31_261+37del (MHRT) | ||
XM_017021340.1:c.4954-30_4954-24del (MYH7) | XP_016876829.1:n.4954-30_4954-24del | |
NM_000257.4:c.4954-30_4954-24del (MYH7) MANE Select | NP_000248.2:n.4954-30_4954-24del |