HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149978577A>G , CM000667.2:g.149978577A>G | GRCh38 |
NC_000005.9:g.149358140A>G , CM000667.1:g.149358140A>G | GRCh37 |
NC_000005.8:g.149338333A>G | NCBI36 |
NG_007147.2:g.19695A>G , LRG_684:g.19695A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000690410.1:n.1157A>G | ||
ENST00000286298.5:c.699+226A>G MANE Select | ENSP00000286298.4:n.699+226A>G | |
ENST00000286298.4:c.699+226A>G | ENSP00000286298.4:n.699+226A>G | |
ENST00000503336.1:c.372+226A>G | ENSP00000426053.1:n.372+226A>G | |
NM_000112.3:c.699+226A>G , LRG_684t1:c.699+226A>G | NP_000103.2:n.699+226A>G | |
XM_017009191.2:c.699+226A>G | XP_016864680.1:n.699+226A>G | |
NM_000112.4:c.699+226A>G MANE Select | NP_000103.2:n.699+226A>G |