HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8076331C>A , CM000679.2:g.8076331C>A | GRCh38 |
NC_000017.10:g.7979649C>A , CM000679.1:g.7979649C>A | GRCh37 |
NC_000017.9:g.7920374C>A | NCBI36 |
NG_007099.1:g.16373G>T | |
NG_007099.2:g.16386G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647874.1:c.1376G>T MANE Select | ENSP00000497784.1:p.Gly459Val | |
ENST00000649809.1:c.440G>T | ENSP00000496845.1:p.Gly147Val | |
ENST00000319144.4:c.1376G>T | ENSP00000315167.4:p.Gly459Val | |
ENST00000577351.5:n.323G>T | ||
ENST00000583276.5:n.760G>T | ||
ENST00000584116.1:n.632G>T | ||
NM_001139.2:c.1376G>T | NP_001130.1:p.Gly459Val | |
NM_001139.3:c.1376G>T MANE Select | NP_001130.1:p.Gly459Val |