HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713547_6713549del , CM000681.2:g.6713547_6713549del | GRCh38 |
NC_000019.9:g.6713558_6713560del , CM000681.1:g.6713558_6713560del | GRCh37 |
NC_000019.8:g.6664558_6664560del | NCBI36 |
NG_009557.1:g.12106_12108del , LRG_27:g.12106_12108del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.651-37_651-35del | ENSP00000512083.1:n.651-37_651-35del | |
ENST00000695692.1:n.61_63del | ||
ENST00000245907.11:c.774-37_774-35del MANE Select | ENSP00000245907.4:n.774-37_774-35del | |
ENST00000245907.10:c.774-37_774-35del | ENSP00000245907.4:n.774-37_774-35del | |
ENST00000595577.1:n.278-37_278-35del | ||
ENST00000597442.5:n.24-37_24-35del | ||
NM_000064.3:c.774-37_774-35del | NP_000055.2:n.774-37_774-35del | |
NM_000064.4:c.774-37_774-35del MANE Select | NP_000055.2:n.774-37_774-35del |