HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713636_6713659del , CM000681.2:g.6713636_6713659del | GRCh38 |
NC_000019.9:g.6713647_6713670del , CM000681.1:g.6713647_6713670del | GRCh37 |
NC_000019.8:g.6664647_6664670del | NCBI36 |
NG_009557.1:g.12009_12032del , LRG_27:g.12009_12032del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.651-134_651-111del | ENSP00000512083.1:n.651-134_651-111del | |
ENST00000245907.11:c.774-134_774-111del MANE Select | ENSP00000245907.4:n.774-134_774-111del | |
ENST00000245907.10:c.774-134_774-111del | ENSP00000245907.4:n.774-134_774-111del | |
ENST00000595577.1:n.278-134_278-111del | ||
ENST00000597442.5:n.23+123_24-111del | ||
NM_000064.3:c.774-134_774-111del | NP_000055.2:n.774-134_774-111del | |
NM_000064.4:c.774-134_774-111del MANE Select | NP_000055.2:n.774-134_774-111del |