Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46773866G>C , CM000679.2:g.46773866G>C | GRCh38 |
| NC_000017.10:g.44851232G>C , CM000679.1:g.44851232G>C | GRCh37 |
| NC_000017.9:g.42206395G>C | NCBI36 |
| NG_008084.2:g.49851C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706495.1:c.-72C>G (WNT3) | ENSP00000516418.1:n.-72C>G | |
| ENST00000225512.6:c.124C>G (WNT3) MANE Select | ENSP00000225512.5:p.Pro42Ala | |
| ENST00000225512.5:c.124C>G (WNT3) | ENSP00000225512.5:p.Pro42Ala | |
| ENST00000573788.5:n.535C>G (WNT3) | ||
| NM_030753.4:c.124C>G (WNT3) | NP_110380.1:p.Pro42Ala | |
| XM_024450773.1:c.4809+223347G>C (LRRC37A2) | XP_024306541.1:n.4809+223347G>C | |
| NM_030753.5:c.124C>G (WNT3) MANE Select | NP_110380.1:p.Pro42Ala |