Canonical Allele Identifier: CA2262401183
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs9890413

Genomic Alleles

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

Transcript Alleles

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