Canonical Allele Identifier: CA2262378096
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773645C= , CM000679.2:g.46773645C= GRCh38
NC_000017.10:g.44851011C= , CM000679.1:g.44851011C= GRCh37
NC_000017.9:g.42206174C= NCBI36
NG_008084.2:g.50072G=

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+23G= (WNT3) ENSP00000516418.1:n.127+23G=
ENST00000225512.6:c.322+23G= (WNT3) MANE Select ENSP00000225512.5:n.322+23G=
ENST00000225512.5:c.322+23G= (WNT3) ENSP00000225512.5:n.322+23G=
NM_030753.4:c.322+23G= (WNT3) NP_110380.1:n.322+23G=
XM_024450773.1:c.4809+223126C= (LRRC37A2) XP_024306541.1:n.4809+223126C=
NM_030753.5:c.322+23G= (WNT3) MANE Select NP_110380.1:n.322+23G=