HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479952del , CM000669.2:g.117479952del | GRCh38 |
NC_000007.13:g.117120006del , CM000669.1:g.117120006del | GRCh37 |
NC_000007.12:g.116907242del | NCBI36 |
NG_016465.4:g.19169del , LRG_663:g.19169del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000446805.2:c.-191+258del | ENSP00000417012.1:n.-191+258del | |
ENST00000673785.1:c.-406+14121del | ENSP00000501235.1:n.-406+14121del | |
ENST00000446805.1:c.-191+258del | ENSP00000417012.1:n.-191+258del | |
ENST00000546407.1:n.166+4144del | ||
XM_011515751.1:c.143+607del | XP_011514053.1:n.143+607del | |
XM_011515752.1:c.143+607del | XP_011514054.1:n.143+607del | |
XM_011515753.1:c.-191+258del | XP_011514055.1:n.-191+258del | |
XM_011515754.1:c.-518-196del | XP_011514056.1:n.-518-196del |