HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479490A>T , CM000669.2:g.117479490A>T | GRCh38 |
NC_000007.13:g.117119544A>T , CM000669.1:g.117119544A>T | GRCh37 |
NC_000007.12:g.116906780A>T | NCBI36 |
NG_016465.4:g.18707A>T , LRG_663:g.18707A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000446805.2:c.-395A>T | ENSP00000417012.1:n.-395A>T | |
ENST00000673785.1:c.-406+13659A>T | ENSP00000501235.1:n.-406+13659A>T | |
ENST00000446805.1:c.-395A>T | ENSP00000417012.1:n.-395A>T | |
ENST00000546407.1:n.166+3682A>T | ||
XM_011515751.1:c.143+145A>T | XP_011514053.1:n.143+145A>T | |
XM_011515752.1:c.143+145A>T | XP_011514054.1:n.143+145A>T | |
XM_011515753.1:c.-395A>T | XP_011514055.1:n.-395A>T | |
XM_011515754.1:c.-723A>T | XP_011514056.1:n.-723A>T |