Canonical Allele Identifier: CA2262378107
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs2059392731
gnomAD v4: 17-46773651-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773651C>A , CM000679.2:g.46773651C>A GRCh38
NC_000017.10:g.44851017C>A , CM000679.1:g.44851017C>A GRCh37
NC_000017.9:g.42206180C>A NCBI36
NG_008084.2:g.50066G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.127+17G>T (WNT3) ENSP00000516418.1:n.127+17G>T
ENST00000225512.6:c.322+17G>T (WNT3) MANE Select ENSP00000225512.5:n.322+17G>T
ENST00000225512.5:c.322+17G>T (WNT3) ENSP00000225512.5:n.322+17G>T
NM_030753.4:c.322+17G>T (WNT3) NP_110380.1:n.322+17G>T
XM_024450773.1:c.4809+223132C>A (LRRC37A2) XP_024306541.1:n.4809+223132C>A
NM_030753.5:c.322+17G>T (WNT3) MANE Select NP_110380.1:n.322+17G>T
Search 100 bp 5'
Search 100 bp 3'