HGVS | Genome Assembly |
---|---|
NC_000017.11:g.46773877A>G , CM000679.2:g.46773877A>G | GRCh38 |
NC_000017.10:g.44851243A>G , CM000679.1:g.44851243A>G | GRCh37 |
NC_000017.9:g.42206406A>G | NCBI36 |
NG_008084.2:g.49840T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706495.1:c.-83T>C (WNT3) | ENSP00000516418.1:n.-83T>C | |
ENST00000225512.6:c.113T>C (WNT3) MANE Select | ENSP00000225512.5:p.Leu38Pro | |
ENST00000225512.5:c.113T>C (WNT3) | ENSP00000225512.5:p.Leu38Pro | |
ENST00000573788.5:n.524T>C (WNT3) | ||
NM_030753.4:c.113T>C (WNT3) | NP_110380.1:p.Leu38Pro | |
XM_024450773.1:c.4809+223358A>G (LRRC37A2) | XP_024306541.1:n.4809+223358A>G | |
NM_030753.5:c.113T>C (WNT3) MANE Select | NP_110380.1:p.Leu38Pro |