Canonical Allele Identifier: CA772510257

Gene: WNT3 LRRC37A2

Linked Data

• dbSNP Id: rs1288763332
• gnomAD v3: 17-46774037-T-C
• gnomAD v4: 17-46774037-T-C
• MyVariant Identifiers: chr17:g.44851403T>C (hg19) ; chr17:g.46774037T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46774037T>C , CM000679.2:g.46774037T>C	GRCh38
NC_000017.10:g.44851403T>C , CM000679.1:g.44851403T>C	GRCh37
NC_000017.9:g.42206566T>C	NCBI36
NG_008084.2:g.49680A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.-115-128A>G (WNT3)	ENSP00000516418.1:n.-115-128A>G
ENST00000225512.6:c.81-128A>G (WNT3) MANE Select	ENSP00000225512.5:n.81-128A>G
ENST00000225512.5:c.81-128A>G (WNT3)	ENSP00000225512.5:n.81-128A>G
ENST00000573788.5:n.492-128A>G (WNT3)
NM_030753.4:c.81-128A>G (WNT3)	NP_110380.1:n.81-128A>G
XM_024450773.1:c.4809+223518T>C (LRRC37A2)	XP_024306541.1:n.4809+223518T>C
NM_030753.5:c.81-128A>G (WNT3) MANE Select	NP_110380.1:n.81-128A>G