HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149981054A>G , CM000667.2:g.149981054A>G | GRCh38 |
NC_000005.9:g.149360617A>G , CM000667.1:g.149360617A>G | GRCh37 |
NC_000005.8:g.149340810A>G | NCBI36 |
NG_007147.2:g.22172A>G , LRG_684:g.22172A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.1461A>G MANE Select | ENSP00000286298.4:p.Thr487= | |
ENST00000286298.4:c.1461A>G | ENSP00000286298.4:p.Thr487= | |
ENST00000503336.1:c.372+2703A>G | ENSP00000426053.1:n.372+2703A>G | |
NM_000112.3:c.1461A>G , LRG_684t1:c.1461A>G | NP_000103.2:p.Thr487= | |
XM_017009191.2:c.1461A>G | XP_016864680.1:p.Thr487= | |
NM_000112.4:c.1461A>G MANE Select | NP_000103.2:p.Thr487= |