Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48978677C>T , CM000674.2:g.48978677C>T | GRCh38 |
| NC_000012.11:g.49372460C>T , CM000674.1:g.49372460C>T | GRCh37 |
| NC_000012.10:g.47658727C>T | NCBI36 |
| NG_033141.1:g.5225C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005430.4:c.27C>T (WNT1) MANE Select | NP_005421.1:p.Gly9= |
| ENST00000293549.4:c.27C>T (WNT1) MANE Select | ENSP00000293549.3:p.Gly9= |
| NM_005430.3:c.27C>T (WNT1) | NP_005421.1:p.Gly9= |
| ENST00000293549.3:c.27C>T (WNT1) | ENSP00000293549.3:p.Gly9= |
| ENST00000613114.4:c.27C>T (WNT1) | ENSP00000481240.1:p.Gly9= |
| XM_024449179.1:c.-2069+822G>A (WNT10B) | XP_024304947.1:n.-2069+822G>A |