HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479517G= , CM000669.2:g.117479517G= | GRCh38 |
NC_000007.13:g.117119571G= , CM000669.1:g.117119571G= | GRCh37 |
NC_000007.12:g.116906807G= | NCBI36 |
NG_016465.4:g.18734G= , LRG_663:g.18734G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000446805.2:c.-368G= | ENSP00000417012.1:n.-368G= | |
ENST00000673785.1:c.-406+13686G= | ENSP00000501235.1:n.-406+13686G= | |
ENST00000446805.1:c.-368G= | ENSP00000417012.1:n.-368G= | |
ENST00000546407.1:n.166+3709G= | ||
XM_011515751.1:c.143+172G= | XP_011514053.1:n.143+172G= | |
XM_011515752.1:c.143+172G= | XP_011514054.1:n.143+172G= | |
XM_011515753.1:c.-368G= | XP_011514055.1:n.-368G= | |
XM_011515754.1:c.-696G= | XP_011514056.1:n.-696G= |