Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46773854C= , CM000679.2:g.46773854C= | GRCh38 |
| NC_000017.10:g.44851220C= , CM000679.1:g.44851220C= | GRCh37 |
| NC_000017.9:g.42206383C= | NCBI36 |
| NG_008084.2:g.49863G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706495.1:c.-60G= (WNT3) | ENSP00000516418.1:n.-60G= | |
| ENST00000225512.6:c.136G= (WNT3) MANE Select | ENSP00000225512.5:p.Gly46= | |
| ENST00000225512.5:c.136G= (WNT3) | ENSP00000225512.5:p.Gly46= | |
| ENST00000573788.5:n.547G= (WNT3) | ||
| NM_030753.4:c.136G= (WNT3) | NP_110380.1:p.Gly46= | |
| XM_024450773.1:c.4809+223335C= (LRRC37A2) | XP_024306541.1:n.4809+223335C= | |
| NM_030753.5:c.136G= (WNT3) MANE Select | NP_110380.1:p.Gly46= |