HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2787125T>A , CM000686.2:g.2787125T>A | GRCh38 |
NC_000024.9:g.2655166T>A , CM000686.1:g.2655166T>A | GRCh37 |
NC_000024.8:g.2715166T>A | NCBI36 |
NG_011751.1:g.5627A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000679518.1:n.106+12386T>A | ||
ENST00000679825.1:n.237T>A | ||
ENST00000680285.1:n.320-2624T>A | ||
ENST00000680845.1:n.165+72T>A | ||
ENST00000681787.1:n.106+12386T>A | ||
ENST00000681940.1:n.106+12386T>A | ||
ENST00000383070.2:c.479A>T MANE Select | ENSP00000372547.1:p.Asp160Val | |
ENST00000383070.1:c.479A>T | ENSP00000372547.1:p.Asp160Val | |
NM_003140.2:c.479A>T | NP_003131.1:p.Asp160Val | |
NM_003140.3:c.479A>T MANE Select | NP_003131.1:p.Asp160Val |