HGVS | Genome Assembly |
---|---|
NC_000017.11:g.46773902C>T , CM000679.2:g.46773902C>T | GRCh38 |
NC_000017.10:g.44851268C>T , CM000679.1:g.44851268C>T | GRCh37 |
NC_000017.9:g.42206431C>T | NCBI36 |
NG_008084.2:g.49815G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706495.1:c.-108G>A (WNT3) | ENSP00000516418.1:n.-108G>A | |
ENST00000225512.6:c.88G>A (WNT3) MANE Select | ENSP00000225512.5:p.Ala30Thr | |
ENST00000225512.5:c.88G>A (WNT3) | ENSP00000225512.5:p.Ala30Thr | |
ENST00000573788.5:n.499G>A (WNT3) | ||
NM_030753.4:c.88G>A (WNT3) | NP_110380.1:p.Ala30Thr | |
XM_024450773.1:c.4809+223383C>T (LRRC37A2) | XP_024306541.1:n.4809+223383C>T | |
NM_030753.5:c.88G>A (WNT3) MANE Select | NP_110380.1:p.Ala30Thr |