Linked Data
MyVariant Identifiers:
chr17:g.44851176G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46773810G>A , CM000679.2:g.46773810G>A | GRCh38 |
| NC_000017.10:g.44851176G>A , CM000679.1:g.44851176G>A | GRCh37 |
| NC_000017.9:g.42206339G>A | NCBI36 |
| NG_008084.2:g.49907C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706495.1:c.-16C>T (WNT3) | ENSP00000516418.1:n.-16C>T | |
| ENST00000225512.6:c.180C>T (WNT3) MANE Select | ENSP00000225512.5:p.Arg60= | |
| ENST00000225512.5:c.180C>T (WNT3) | ENSP00000225512.5:p.Arg60= | |
| NM_030753.4:c.180C>T (WNT3) | NP_110380.1:p.Arg60= | |
| XM_024450773.1:c.4809+223291G>A (LRRC37A2) | XP_024306541.1:n.4809+223291G>A | |
| NM_030753.5:c.180C>T (WNT3) MANE Select | NP_110380.1:p.Arg60= |