HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479819G>T , CM000669.2:g.117479819G>T | GRCh38 |
NC_000007.13:g.117119873G>T , CM000669.1:g.117119873G>T | GRCh37 |
NC_000007.12:g.116907109G>T | NCBI36 |
NG_016465.4:g.19036G>T , LRG_663:g.19036G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000446805.2:c.-191+125G>T | ENSP00000417012.1:n.-191+125G>T | |
ENST00000673785.1:c.-406+13988G>T | ENSP00000501235.1:n.-406+13988G>T | |
ENST00000446805.1:c.-191+125G>T | ENSP00000417012.1:n.-191+125G>T | |
ENST00000546407.1:n.166+4011G>T | ||
XM_011515751.1:c.143+474G>T | XP_011514053.1:n.143+474G>T | |
XM_011515752.1:c.143+474G>T | XP_011514054.1:n.143+474G>T | |
XM_011515753.1:c.-191+125G>T | XP_011514055.1:n.-191+125G>T | |
XM_011515754.1:c.-519+125G>T | XP_011514056.1:n.-519+125G>T |