HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2787428C>G , CM000686.2:g.2787428C>G | GRCh38 |
NC_000024.9:g.2655469C>G , CM000686.1:g.2655469C>G | GRCh37 |
NC_000024.8:g.2715469C>G | NCBI36 |
NG_011751.1:g.5324G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000679518.1:n.106+12689C>G | ||
ENST00000679825.1:n.540C>G | ||
ENST00000680285.1:n.320-2321C>G | ||
ENST00000680845.1:n.166-52C>G | ||
ENST00000681787.1:n.106+12689C>G | ||
ENST00000681940.1:n.106+12689C>G | ||
ENST00000383070.2:c.176G>C MANE Select | ENSP00000372547.1:p.Arg59Thr | |
ENST00000383070.1:c.176G>C | ENSP00000372547.1:p.Arg59Thr | |
NM_003140.2:c.176G>C | NP_003131.1:p.Arg59Thr | |
NM_003140.3:c.176G>C MANE Select | NP_003131.1:p.Arg59Thr |