HGVS | Genome Assembly |
---|---|
NC_000017.11:g.46773709A>G , CM000679.2:g.46773709A>G | GRCh38 |
NC_000017.10:g.44851075A>G , CM000679.1:g.44851075A>G | GRCh37 |
NC_000017.9:g.42206238A>G | NCBI36 |
NG_008084.2:g.50008T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706495.1:c.86T>C (WNT3) | ENSP00000516418.1:p.Ile29Thr | |
ENST00000225512.6:c.281T>C (WNT3) MANE Select | ENSP00000225512.5:p.Ile94Thr | |
ENST00000225512.5:c.281T>C (WNT3) | ENSP00000225512.5:p.Ile94Thr | |
NM_030753.4:c.281T>C (WNT3) | NP_110380.1:p.Ile94Thr | |
XM_024450773.1:c.4809+223190A>G (LRRC37A2) | XP_024306541.1:n.4809+223190A>G | |
NM_030753.5:c.281T>C (WNT3) MANE Select | NP_110380.1:p.Ile94Thr |