HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479550A>G , CM000669.2:g.117479550A>G | GRCh38 |
NC_000007.13:g.117119604A>G , CM000669.1:g.117119604A>G | GRCh37 |
NC_000007.12:g.116906840A>G | NCBI36 |
NG_016465.4:g.18767A>G , LRG_663:g.18767A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000446805.2:c.-335A>G | ENSP00000417012.1:n.-335A>G | |
ENST00000673785.1:c.-406+13719A>G | ENSP00000501235.1:n.-406+13719A>G | |
ENST00000446805.1:c.-335A>G | ENSP00000417012.1:n.-335A>G | |
ENST00000546407.1:n.166+3742A>G | ||
XM_011515751.1:c.143+205A>G | XP_011514053.1:n.143+205A>G | |
XM_011515752.1:c.143+205A>G | XP_011514054.1:n.143+205A>G | |
XM_011515753.1:c.-335A>G | XP_011514055.1:n.-335A>G | |
XM_011515754.1:c.-663A>G | XP_011514056.1:n.-663A>G |