HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713841_6713863del , CM000681.2:g.6713841_6713863del | GRCh38 |
NC_000019.9:g.6713852_6713874del , CM000681.1:g.6713852_6713874del | GRCh37 |
NC_000019.8:g.6664852_6664874del | NCBI36 |
NG_009557.1:g.11811_11833del , LRG_27:g.11811_11833del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.650+151_650+173del | ENSP00000512083.1:n.650+151_650+173del | |
ENST00000245907.11:c.773+151_773+173del MANE Select | ENSP00000245907.4:n.773+151_773+173del | |
ENST00000245907.10:c.773+151_773+173del | ENSP00000245907.4:n.773+151_773+173del | |
ENST00000595577.1:n.277+151_277+173del | ||
NM_000064.3:c.773+151_773+173del | NP_000055.2:n.773+151_773+173del | |
NM_000064.4:c.773+151_773+173del MANE Select | NP_000055.2:n.773+151_773+173del |