HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713841_6713887del , CM000681.2:g.6713841_6713887del | GRCh38 |
NC_000019.9:g.6713852_6713898del , CM000681.1:g.6713852_6713898del | GRCh37 |
NC_000019.8:g.6664852_6664898del | NCBI36 |
NG_009557.1:g.11785_11831del , LRG_27:g.11785_11831del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.650+125_650+171del | ENSP00000512083.1:n.650+125_650+171del | |
ENST00000245907.11:c.773+125_773+171del MANE Select | ENSP00000245907.4:n.773+125_773+171del | |
ENST00000245907.10:c.773+125_773+171del | ENSP00000245907.4:n.773+125_773+171del | |
ENST00000595577.1:n.277+125_277+171del | ||
NM_000064.3:c.773+125_773+171del | NP_000055.2:n.773+125_773+171del | |
NM_000064.4:c.773+125_773+171del MANE Select | NP_000055.2:n.773+125_773+171del |