Canonical Allele Identifier: CA8620635
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1916811
ClinVar RCV Id: RCV002625425
dbSNP Id: rs200609079
ExAC: 17:44851014 C / G
gnomAD v2: 17-44851014-C-G
gnomAD v3: 17-46773648-C-G
gnomAD v4: 17-46773648-C-G
MyVariant Identifiers: chr17:g.44851014C>G (hg19) chr17:g.44851014_44851016delinsGCT (hg19) chr17:g.46773648C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773648C>G , CM000679.2:g.46773648C>G GRCh38
NC_000017.10:g.44851014C>G , CM000679.1:g.44851014C>G GRCh37
NC_000017.9:g.42206177C>G NCBI36
NG_008084.2:g.50069G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+20G>C (WNT3) ENSP00000516418.1:n.127+20G>C
ENST00000225512.6:c.322+20G>C (WNT3) MANE Select ENSP00000225512.5:n.322+20G>C
ENST00000225512.5:c.322+20G>C (WNT3) ENSP00000225512.5:n.322+20G>C
NM_030753.4:c.322+20G>C (WNT3) NP_110380.1:n.322+20G>C
XM_024450773.1:c.4809+223129C>G (LRRC37A2) XP_024306541.1:n.4809+223129C>G
NM_030753.5:c.322+20G>C (WNT3) MANE Select NP_110380.1:n.322+20G>C
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