HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117478732G>A , CM000669.2:g.117478732G>A | GRCh38 |
NC_000007.13:g.117118786G>A , CM000669.1:g.117118786G>A | GRCh37 |
NC_000007.12:g.116906022G>A | NCBI36 |
NG_016465.4:g.17949G>A , LRG_663:g.17949G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000446805.2:c.-526+310G>A | ENSP00000417012.1:n.-526+310G>A | |
ENST00000673785.1:c.-406+12901G>A | ENSP00000501235.1:n.-406+12901G>A | |
ENST00000546407.1:n.166+2924G>A | ||
XM_011515751.1:c.41+310G>A | XP_011514053.1:n.41+310G>A | |
XM_011515752.1:c.41+310G>A | XP_011514054.1:n.41+310G>A | |
XM_011515754.1:c.-1365G>A | XP_011514056.1:n.-1365G>A |