HGVS | Genome Assembly |
---|---|
NC_000017.11:g.5022371T>A , CM000679.2:g.5022371T>A | GRCh38 |
NC_000017.10:g.4925666T>A , CM000679.1:g.4925666T>A | GRCh37 |
NC_000017.9:g.4866390T>A | NCBI36 |
NG_034137.1:g.29424T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320785.10:c.2290T>A MANE Select | ENSP00000320821.5:p.Phe764Ile | |
ENST00000320785.9:c.2290T>A | ENSP00000320821.5:p.Phe764Ile | |
NM_006612.5:c.2290T>A | NP_006603.2:p.Phe764Ile | |
XM_005256424.1:c.2290T>A | XP_005256481.1:p.Phe764Ile | |
XM_005256424.2:c.2290T>A | XP_005256481.1:p.Phe764Ile | |
NM_006612.6:c.2290T>A MANE Select | NP_006603.2:p.Phe764Ile |