HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149980566T>A , CM000667.2:g.149980566T>A | GRCh38 |
NC_000005.9:g.149360129T>A , CM000667.1:g.149360129T>A | GRCh37 |
NC_000005.8:g.149340322T>A | NCBI36 |
NG_007147.2:g.21684T>A , LRG_684:g.21684T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286298.5:c.973T>A MANE Select | ENSP00000286298.4:p.Phe325Ile | |
ENST00000286298.4:c.973T>A | ENSP00000286298.4:p.Phe325Ile | |
ENST00000503336.1:c.372+2215T>A | ENSP00000426053.1:n.372+2215T>A | |
NM_000112.3:c.973T>A , LRG_684t1:c.973T>A | NP_000103.2:p.Phe325Ile | |
XM_017009191.2:c.973T>A | XP_016864680.1:p.Phe325Ile | |
NM_000112.4:c.973T>A MANE Select | NP_000103.2:p.Phe325Ile |