Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46773650T>C , CM000679.2:g.46773650T>C | GRCh38 |
| NC_000017.10:g.44851016T>C , CM000679.1:g.44851016T>C | GRCh37 |
| NC_000017.9:g.42206179T>C | NCBI36 |
| NG_008084.2:g.50067A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_030753.5:c.322+18A>G (WNT3) MANE Select | NP_110380.1:n.322+18A>G |
| ENST00000225512.6:c.322+18A>G (WNT3) MANE Select | ENSP00000225512.5:n.322+18A>G |
| NM_030753.4:c.322+18A>G (WNT3) | NP_110380.1:n.322+18A>G |
| ENST00000225512.5:c.322+18A>G (WNT3) | ENSP00000225512.5:n.322+18A>G |
| ENST00000706495.1:c.127+18A>G (WNT3) | ENSP00000516418.1:n.127+18A>G |
| XM_024450773.1:c.4809+223131T>C (LRRC37A2) | XP_024306541.1:n.4809+223131T>C |