Canonical Allele Identifier: CA2262401184
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs9890413
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46824083G>T , CM000679.2:g.46824083G>T GRCh38
NC_000017.10:g.44901449G>T , CM000679.1:g.44901449G>T GRCh37
NC_000017.9:g.42256448G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.-116+7365C>A (WNT3) ENSP00000516418.1:n.-116+7365C>A
ENST00000573788.5:n.386-2870C>A (WNT3)
XM_024450773.1:c.4810-224973G>T (LRRC37A2) XP_024306541.1:n.4810-224973G>T
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