HGVS | Genome Assembly |
---|---|
NC_000017.11:g.46773840G>A , CM000679.2:g.46773840G>A | GRCh38 |
NC_000017.10:g.44851206G>A , CM000679.1:g.44851206G>A | GRCh37 |
NC_000017.9:g.42206369G>A | NCBI36 |
NG_008084.2:g.49877C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706495.1:c.-46C>T (WNT3) | ENSP00000516418.1:n.-46C>T | |
ENST00000225512.6:c.150C>T (WNT3) MANE Select | ENSP00000225512.5:p.Gly50= | |
ENST00000225512.5:c.150C>T (WNT3) | ENSP00000225512.5:p.Gly50= | |
NM_030753.4:c.150C>T (WNT3) | NP_110380.1:p.Gly50= | |
XM_024450773.1:c.4809+223321G>A (LRRC37A2) | XP_024306541.1:n.4809+223321G>A | |
NM_030753.5:c.150C>T (WNT3) MANE Select | NP_110380.1:p.Gly50= |