Canonical Allele Identifier: CA400011550
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773850G>A , CM000679.2:g.46773850G>A GRCh38
NC_000017.10:g.44851216G>A , CM000679.1:g.44851216G>A GRCh37
NC_000017.9:g.42206379G>A NCBI36
NG_008084.2:g.49867C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-56C>T (WNT3) ENSP00000516418.1:n.-56C>T
ENST00000225512.6:c.140C>T (WNT3) MANE Select ENSP00000225512.5:p.Ser47Phe
ENST00000225512.5:c.140C>T (WNT3) ENSP00000225512.5:p.Ser47Phe
ENST00000573788.5:n.551C>T (WNT3)
NM_030753.4:c.140C>T (WNT3) NP_110380.1:p.Ser47Phe
XM_024450773.1:c.4809+223331G>A (LRRC37A2) XP_024306541.1:n.4809+223331G>A
NM_030753.5:c.140C>T (WNT3) MANE Select NP_110380.1:p.Ser47Phe