HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117478746G= , CM000669.2:g.117478746G= | GRCh38 |
NC_000007.13:g.117118800G= , CM000669.1:g.117118800G= | GRCh37 |
NC_000007.12:g.116906036G= | NCBI36 |
NG_016465.4:g.17963G= , LRG_663:g.17963G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000446805.2:c.-526+324G= | ENSP00000417012.1:n.-526+324G= | |
ENST00000673785.1:c.-406+12915G= | ENSP00000501235.1:n.-406+12915G= | |
ENST00000546407.1:n.166+2938G= | ||
XM_011515751.1:c.41+324G= | XP_011514053.1:n.41+324G= | |
XM_011515752.1:c.41+324G= | XP_011514054.1:n.41+324G= | |
XM_011515754.1:c.-1351G= | XP_011514056.1:n.-1351G= |