HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713675_6713676del , CM000681.2:g.6713675_6713676del | GRCh38 |
NC_000019.9:g.6713686_6713687del , CM000681.1:g.6713686_6713687del | GRCh37 |
NC_000019.8:g.6664686_6664687del | NCBI36 |
NG_009557.1:g.11976_11977del , LRG_27:g.11976_11977del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.651-167_651-166del | ENSP00000512083.1:n.651-167_651-166del | |
ENST00000245907.11:c.774-167_774-166del MANE Select | ENSP00000245907.4:n.774-167_774-166del | |
ENST00000245907.10:c.774-167_774-166del | ENSP00000245907.4:n.774-167_774-166del | |
ENST00000595577.1:n.278-167_278-166del | ||
ENST00000597442.5:n.23+90_23+91del | ||
NM_000064.3:c.774-167_774-166del | NP_000055.2:n.774-167_774-166del | |
NM_000064.4:c.774-167_774-166del MANE Select | NP_000055.2:n.774-167_774-166del |