HGVS | Genome Assembly |
---|---|
NC_000017.11:g.46773645C= , CM000679.2:g.46773645C= | GRCh38 |
NC_000017.10:g.44851011C= , CM000679.1:g.44851011C= | GRCh37 |
NC_000017.9:g.42206174C= | NCBI36 |
NG_008084.2:g.50072G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000706495.1:c.127+23G= (WNT3) | ENSP00000516418.1:n.127+23G= | |
ENST00000225512.6:c.322+23G= (WNT3) MANE Select | ENSP00000225512.5:n.322+23G= | |
ENST00000225512.5:c.322+23G= (WNT3) | ENSP00000225512.5:n.322+23G= | |
NM_030753.4:c.322+23G= (WNT3) | NP_110380.1:n.322+23G= | |
XM_024450773.1:c.4809+223126C= (LRRC37A2) | XP_024306541.1:n.4809+223126C= | |
NM_030753.5:c.322+23G= (WNT3) MANE Select | NP_110380.1:n.322+23G= |