HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479397del , CM000669.2:g.117479397del | GRCh38 |
NC_000007.13:g.117119451del , CM000669.1:g.117119451del | GRCh37 |
NC_000007.12:g.116906687del | NCBI36 |
NG_016465.4:g.18614del , LRG_663:g.18614del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000446805.2:c.-424+52del | ENSP00000417012.1:n.-424+52del | |
ENST00000673785.1:c.-406+13566del | ENSP00000501235.1:n.-406+13566del | |
ENST00000446805.1:c.-424+52del | ENSP00000417012.1:n.-424+52del | |
ENST00000546407.1:n.166+3589del | ||
XM_011515751.1:c.143+52del | XP_011514053.1:n.143+52del | |
XM_011515752.1:c.143+52del | XP_011514054.1:n.143+52del | |
XM_011515753.1:c.-424+52del | XP_011514055.1:n.-424+52del | |
XM_011515754.1:c.-752+52del | XP_011514056.1:n.-752+52del |