HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479804A>T , CM000669.2:g.117479804A>T | GRCh38 |
NC_000007.13:g.117119858A>T , CM000669.1:g.117119858A>T | GRCh37 |
NC_000007.12:g.116907094A>T | NCBI36 |
NG_016465.4:g.19021A>T , LRG_663:g.19021A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000446805.2:c.-191+110A>T | ENSP00000417012.1:n.-191+110A>T | |
ENST00000673785.1:c.-406+13973A>T | ENSP00000501235.1:n.-406+13973A>T | |
ENST00000446805.1:c.-191+110A>T | ENSP00000417012.1:n.-191+110A>T | |
ENST00000546407.1:n.166+3996A>T | ||
XM_011515751.1:c.143+459A>T | XP_011514053.1:n.143+459A>T | |
XM_011515752.1:c.143+459A>T | XP_011514054.1:n.143+459A>T | |
XM_011515753.1:c.-191+110A>T | XP_011514055.1:n.-191+110A>T | |
XM_011515754.1:c.-519+110A>T | XP_011514056.1:n.-519+110A>T |