HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734426A>T , CM000679.2:g.4734426A>T | GRCh38 |
NC_000017.10:g.4637721A>T , CM000679.1:g.4637721A>T | GRCh37 |
NC_000017.9:g.4584470A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*77T>A MANE Select | ENSP00000293778.7:n.*77T>A | |
ENST00000574412.6:c.*180T>A | ENSP00000459592.2:n.*180T>A | |
ENST00000293778.10:c.*77T>A | ENSP00000293778.6:n.*77T>A | |
ENST00000574412.5:c.*180T>A | ENSP00000459592.1:n.*180T>A | |
ENST00000576153.5:n.633T>A | ||
NM_022059.3:c.*77T>A | NP_071342.2:n.*77T>A | |
NM_022059.4:c.*77T>A | NP_071342.2:n.*77T>A | |
NM_001386809.1:c.*77T>A MANE Select | NP_001373738.1:n.*77T>A |