HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2787365A>G , CM000686.2:g.2787365A>G | GRCh38 |
NC_000024.9:g.2655406A>G , CM000686.1:g.2655406A>G | GRCh37 |
NC_000024.8:g.2715406A>G | NCBI36 |
NG_011751.1:g.5387T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000679518.1:n.106+12626A>G | ||
ENST00000679825.1:n.477A>G | ||
ENST00000680285.1:n.320-2384A>G | ||
ENST00000680845.1:n.166-115A>G | ||
ENST00000681787.1:n.106+12626A>G | ||
ENST00000681940.1:n.106+12626A>G | ||
ENST00000383070.2:c.239T>C MANE Select | ENSP00000372547.1:p.Leu80Pro | |
ENST00000383070.1:c.239T>C | ENSP00000372547.1:p.Leu80Pro | |
NM_003140.2:c.239T>C | NP_003131.1:p.Leu80Pro | |
NM_003140.3:c.239T>C MANE Select | NP_003131.1:p.Leu80Pro |