Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46773785C>A , CM000679.2:g.46773785C>A | GRCh38 |
| NC_000017.10:g.44851151C>A , CM000679.1:g.44851151C>A | GRCh37 |
| NC_000017.9:g.42206314C>A | NCBI36 |
| NG_008084.2:g.49932G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706495.1:c.10G>T (WNT3) | ENSP00000516418.1:p.Val4Leu | |
| ENST00000225512.6:c.205G>T (WNT3) MANE Select | ENSP00000225512.5:p.Val69Leu | |
| ENST00000225512.5:c.205G>T (WNT3) | ENSP00000225512.5:p.Val69Leu | |
| NM_030753.4:c.205G>T (WNT3) | NP_110380.1:p.Val69Leu | |
| XM_024450773.1:c.4809+223266C>A (LRRC37A2) | XP_024306541.1:n.4809+223266C>A | |
| NM_030753.5:c.205G>T (WNT3) MANE Select | NP_110380.1:p.Val69Leu |