HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2787385A= , CM000686.2:g.2787385A= | GRCh38 |
NC_000024.9:g.2655426A= , CM000686.1:g.2655426A= | GRCh37 |
NC_000024.8:g.2715426A= | NCBI36 |
NG_011751.1:g.5367T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000679518.1:n.106+12646A= | ||
ENST00000679825.1:n.497A= | ||
ENST00000680285.1:n.320-2364A= | ||
ENST00000680845.1:n.166-95A= | ||
ENST00000681787.1:n.106+12646A= | ||
ENST00000681940.1:n.106+12646A= | ||
ENST00000383070.2:c.219T= MANE Select | ENSP00000372547.1:p.Asp73= | |
ENST00000383070.1:c.219T= | ENSP00000372547.1:p.Asp73= | |
NM_003140.2:c.219T= | NP_003131.1:p.Asp73= | |
NM_003140.3:c.219T= MANE Select | NP_003131.1:p.Asp73= |