HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479474G= , CM000669.2:g.117479474G= | GRCh38 |
NC_000007.13:g.117119528G= , CM000669.1:g.117119528G= | GRCh37 |
NC_000007.12:g.116906764G= | NCBI36 |
NG_016465.4:g.18691G= , LRG_663:g.18691G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000446805.2:c.-411G= | ENSP00000417012.1:n.-411G= | |
ENST00000673785.1:c.-406+13643G= | ENSP00000501235.1:n.-406+13643G= | |
ENST00000446805.1:c.-411G= | ENSP00000417012.1:n.-411G= | |
ENST00000546407.1:n.166+3666G= | ||
XM_011515751.1:c.143+129G= | XP_011514053.1:n.143+129G= | |
XM_011515752.1:c.143+129G= | XP_011514054.1:n.143+129G= | |
XM_011515753.1:c.-411G= | XP_011514055.1:n.-411G= | |
XM_011515754.1:c.-739G= | XP_011514056.1:n.-739G= |