HGVS | Genome Assembly |
---|---|
NC_000006.12:g.38683102_38683104del , CM000668.2:g.38683102_38683104del | GRCh38 |
NC_000006.11:g.38650878_38650880del , CM000668.1:g.38650878_38650880del | GRCh37 |
NC_000006.10:g.38758856_38758858del | NCBI36 |
NG_012074.1:g.25078_25080del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373365.5:c.309-224_309-222del MANE Select | ENSP00000362463.3:n.309-224_309-222del | |
ENST00000373365.4:c.309-224_309-222del | ENSP00000362463.3:n.309-224_309-222del | |
ENST00000470973.1:n.117_119del | ||
NM_006708.2:c.309-224_309-222del | NP_006699.2:n.309-224_309-222del | |
NM_006708.3:c.309-224_309-222del MANE Select | NP_006699.2:n.309-224_309-222del |