Canonical Allele Identifier: CA772518976

Gene: WNT3 LRRC37A2

Linked Data

• dbSNP Id: rs1365740953
• gnomAD v3: 17-46788308-C-A
• gnomAD v4: 17-46788308-C-A
• MyVariant Identifiers: chr17:g.44865674C>A (hg19) ; chr17:g.46788308C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46788308C>A , CM000679.2:g.46788308C>A	GRCh38
NC_000017.10:g.44865674C>A , CM000679.1:g.44865674C>A	GRCh37
NC_000017.9:g.42220834C>A	NCBI36
NG_008084.2:g.35409G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.-115-14399G>T (WNT3)	ENSP00000516418.1:n.-115-14399G>T
ENST00000225512.6:c.81-14399G>T (WNT3) MANE Select	ENSP00000225512.5:n.81-14399G>T
ENST00000225512.5:c.81-14399G>T (WNT3)	ENSP00000225512.5:n.81-14399G>T
ENST00000573788.5:n.492-14399G>T (WNT3)
NM_030753.4:c.81-14399G>T (WNT3)	NP_110380.1:n.81-14399G>T
XM_024450773.1:c.4809+237789C>A (LRRC37A2)	XP_024306541.1:n.4809+237789C>A
NM_030753.5:c.81-14399G>T (WNT3) MANE Select	NP_110380.1:n.81-14399G>T