Linked Data
dbSNP Id:
rs141487898
gnomAD v2:
17-44865542-C-T
gnomAD v3:
17-46788176-C-T
gnomAD v4:
17-46788176-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46788176C>T , CM000679.2:g.46788176C>T | GRCh38 |
| NC_000017.10:g.44865542C>T , CM000679.1:g.44865542C>T | GRCh37 |
| NC_000017.9:g.42220702C>T | NCBI36 |
| NG_008084.2:g.35541G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000706495.1:c.-115-14267G>A (WNT3) | ENSP00000516418.1:n.-115-14267G>A | |
| ENST00000225512.6:c.81-14267G>A (WNT3) MANE Select | ENSP00000225512.5:n.81-14267G>A | |
| ENST00000225512.5:c.81-14267G>A (WNT3) | ENSP00000225512.5:n.81-14267G>A | |
| ENST00000573788.5:n.492-14267G>A (WNT3) | ||
| NM_030753.4:c.81-14267G>A (WNT3) | NP_110380.1:n.81-14267G>A | |
| XM_024450773.1:c.4809+237657C>T (LRRC37A2) | XP_024306541.1:n.4809+237657C>T | |
| NM_030753.5:c.81-14267G>A (WNT3) MANE Select | NP_110380.1:n.81-14267G>A |