HGVS | Genome Assembly |
---|---|
NC_000017.11:g.46773847A>C , CM000679.2:g.46773847A>C | GRCh38 |
NC_000017.10:g.44851213A>C , CM000679.1:g.44851213A>C | GRCh37 |
NC_000017.9:g.42206376A>C | NCBI36 |
NG_008084.2:g.49870T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706495.1:c.-53T>G (WNT3) | ENSP00000516418.1:n.-53T>G | |
ENST00000225512.6:c.143T>G (WNT3) MANE Select | ENSP00000225512.5:p.Ile48Ser | |
ENST00000225512.5:c.143T>G (WNT3) | ENSP00000225512.5:p.Ile48Ser | |
ENST00000573788.5:n.554T>G (WNT3) | ||
NM_030753.4:c.143T>G (WNT3) | NP_110380.1:p.Ile48Ser | |
XM_024450773.1:c.4809+223328A>C (LRRC37A2) | XP_024306541.1:n.4809+223328A>C | |
NM_030753.5:c.143T>G (WNT3) MANE Select | NP_110380.1:p.Ile48Ser |