HGVS | Genome Assembly |
---|---|
NC_000017.11:g.46773889T>A , CM000679.2:g.46773889T>A | GRCh38 |
NC_000017.10:g.44851255T>A , CM000679.1:g.44851255T>A | GRCh37 |
NC_000017.9:g.42206418T>A | NCBI36 |
NG_008084.2:g.49828A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706495.1:c.-95A>T (WNT3) | ENSP00000516418.1:n.-95A>T | |
ENST00000225512.6:c.101A>T (WNT3) MANE Select | ENSP00000225512.5:p.Gln34Leu | |
ENST00000225512.5:c.101A>T (WNT3) | ENSP00000225512.5:p.Gln34Leu | |
ENST00000573788.5:n.512A>T (WNT3) | ||
NM_030753.4:c.101A>T (WNT3) | NP_110380.1:p.Gln34Leu | |
XM_024450773.1:c.4809+223370T>A (LRRC37A2) | XP_024306541.1:n.4809+223370T>A | |
NM_030753.5:c.101A>T (WNT3) MANE Select | NP_110380.1:p.Gln34Leu |