HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2787561C>A , CM000686.2:g.2787561C>A | GRCh38 |
NC_000024.9:g.2655602C>A , CM000686.1:g.2655602C>A | GRCh37 |
NC_000024.8:g.2715602C>A | NCBI36 |
NG_011751.1:g.5191G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000679518.1:n.106+12822C>A | ||
ENST00000679825.1:n.673C>A | ||
ENST00000680285.1:n.320-2188C>A | ||
ENST00000680845.1:n.247C>A | ||
ENST00000681787.1:n.106+12822C>A | ||
ENST00000681940.1:n.106+12822C>A | ||
ENST00000383070.2:c.43G>T MANE Select | ENSP00000372547.1:p.Asp15Tyr | |
ENST00000383070.1:c.43G>T | ENSP00000372547.1:p.Asp15Tyr | |
NM_003140.2:c.43G>T | NP_003131.1:p.Asp15Tyr | |
NM_003140.3:c.43G>T MANE Select | NP_003131.1:p.Asp15Tyr |