HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49447870_49447958del , CM000668.2:g.49447870_49447958del | GRCh38 |
NC_000006.11:g.49415583_49415671del , CM000668.1:g.49415583_49415671del | GRCh37 |
NC_000006.10:g.49523542_49523630del | NCBI36 |
NG_007100.1:g.20182_20270del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.1445-173_1445-85del MANE Select | ENSP00000274813.3:n.1445-173_1445-85del | |
ENST00000274813.3:c.1445-173_1445-85del | ENSP00000274813.3:n.1445-173_1445-85del | |
NM_000255.3:c.1445-173_1445-85del | NP_000246.2:n.1445-173_1445-85del | |
XM_005249143.2:c.1445-173_1445-85del | XP_005249200.1:n.1445-173_1445-85del | |
XM_005249143.3:c.1445-173_1445-85del | XP_005249200.1:n.1445-173_1445-85del | |
NM_000255.4:c.1445-173_1445-85del MANE Select | NP_000246.2:n.1445-173_1445-85del |