HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117478779T>G , CM000669.2:g.117478779T>G | GRCh38 |
NC_000007.13:g.117118833T>G , CM000669.1:g.117118833T>G | GRCh37 |
NC_000007.12:g.116906069T>G | NCBI36 |
NG_016465.4:g.17996T>G , LRG_663:g.17996T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000446805.2:c.-526+357T>G | ENSP00000417012.1:n.-526+357T>G | |
ENST00000673785.1:c.-406+12948T>G | ENSP00000501235.1:n.-406+12948T>G | |
ENST00000546407.1:n.166+2971T>G | ||
XM_011515751.1:c.41+357T>G | XP_011514053.1:n.41+357T>G | |
XM_011515752.1:c.41+357T>G | XP_011514054.1:n.41+357T>G | |
XM_011515754.1:c.-1318T>G | XP_011514056.1:n.-1318T>G |