HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2787350A= , CM000686.2:g.2787350A= | GRCh38 |
NC_000024.9:g.2655391A= , CM000686.1:g.2655391A= | GRCh37 |
NC_000024.8:g.2715391A= | NCBI36 |
NG_011751.1:g.5402T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000679518.1:n.106+12611A= | ||
ENST00000679825.1:n.462A= | ||
ENST00000680285.1:n.320-2399A= | ||
ENST00000680845.1:n.166-130A= | ||
ENST00000681787.1:n.106+12611A= | ||
ENST00000681940.1:n.106+12611A= | ||
ENST00000383070.2:c.254T= MANE Select | ENSP00000372547.1:p.Met85= | |
ENST00000383070.1:c.254T= | ENSP00000372547.1:p.Met85= | |
NM_003140.2:c.254T= | NP_003131.1:p.Met85= | |
NM_003140.3:c.254T= MANE Select | NP_003131.1:p.Met85= |