Linked Data
MyVariant Identifiers:
chr17:g.44851242C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46773876C>T , CM000679.2:g.46773876C>T | GRCh38 |
| NC_000017.10:g.44851242C>T , CM000679.1:g.44851242C>T | GRCh37 |
| NC_000017.9:g.42206405C>T | NCBI36 |
| NG_008084.2:g.49841G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706495.1:c.-82G>A (WNT3) | ENSP00000516418.1:n.-82G>A | |
| ENST00000225512.6:c.114G>A (WNT3) MANE Select | ENSP00000225512.5:p.Leu38= | |
| ENST00000225512.5:c.114G>A (WNT3) | ENSP00000225512.5:p.Leu38= | |
| ENST00000573788.5:n.525G>A (WNT3) | ||
| NM_030753.4:c.114G>A (WNT3) | NP_110380.1:p.Leu38= | |
| XM_024450773.1:c.4809+223357C>T (LRRC37A2) | XP_024306541.1:n.4809+223357C>T | |
| NM_030753.5:c.114G>A (WNT3) MANE Select | NP_110380.1:p.Leu38= |