Canonical Allele Identifier: CA2262378261
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs1021092843
gnomAD v4: 17-46774052-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46774052C>A , CM000679.2:g.46774052C>A GRCh38
NC_000017.10:g.44851418C>A , CM000679.1:g.44851418C>A GRCh37
NC_000017.9:g.42206581C>A NCBI36
NG_008084.2:g.49665G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-115-143G>T (WNT3) ENSP00000516418.1:n.-115-143G>T
ENST00000225512.6:c.81-143G>T (WNT3) MANE Select ENSP00000225512.5:n.81-143G>T
ENST00000225512.5:c.81-143G>T (WNT3) ENSP00000225512.5:n.81-143G>T
ENST00000573788.5:n.492-143G>T (WNT3)
NM_030753.4:c.81-143G>T (WNT3) NP_110380.1:n.81-143G>T
XM_024450773.1:c.4809+223533C>A (LRRC37A2) XP_024306541.1:n.4809+223533C>A
NM_030753.5:c.81-143G>T (WNT3) MANE Select NP_110380.1:n.81-143G>T
Search 100 bp 5'
Search 100 bp 3'