HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49447859del , CM000668.2:g.49447859del | GRCh38 |
NC_000006.11:g.49415572del , CM000668.1:g.49415572del | GRCh37 |
NC_000006.10:g.49523531del | NCBI36 |
NG_007100.1:g.20284del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.1445-71del MANE Select | ENSP00000274813.3:n.1445-71del | |
ENST00000274813.3:c.1445-71del | ENSP00000274813.3:n.1445-71del | |
NM_000255.3:c.1445-71del | NP_000246.2:n.1445-71del | |
XM_005249143.2:c.1445-71del | XP_005249200.1:n.1445-71del | |
XM_005249143.3:c.1445-71del | XP_005249200.1:n.1445-71del | |
NM_000255.4:c.1445-71del MANE Select | NP_000246.2:n.1445-71del |