HGVS | Genome Assembly |
---|---|
NC_000017.11:g.46773649C>A , CM000679.2:g.46773649C>A | GRCh38 |
NC_000017.10:g.44851015C>A , CM000679.1:g.44851015C>A | GRCh37 |
NC_000017.9:g.42206178C>A | NCBI36 |
NG_008084.2:g.50068G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000706495.1:c.127+19G>T (WNT3) | ENSP00000516418.1:n.127+19G>T | |
ENST00000225512.6:c.322+19G>T (WNT3) MANE Select | ENSP00000225512.5:n.322+19G>T | |
ENST00000225512.5:c.322+19G>T (WNT3) | ENSP00000225512.5:n.322+19G>T | |
NM_030753.4:c.322+19G>T (WNT3) | NP_110380.1:n.322+19G>T | |
XM_024450773.1:c.4809+223130C>A (LRRC37A2) | XP_024306541.1:n.4809+223130C>A | |
NM_030753.5:c.322+19G>T (WNT3) MANE Select | NP_110380.1:n.322+19G>T |