Canonical Allele Identifier: CA2638404116

Gene: WNT3 LRRC37A2

Linked Data

• gnomAD v4: 17-46773979-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46773979C>G , CM000679.2:g.46773979C>G	GRCh38
NC_000017.10:g.44851345C>G , CM000679.1:g.44851345C>G	GRCh37
NC_000017.9:g.42206508C>G	NCBI36
NG_008084.2:g.49738G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.-115-70G>C (WNT3)	ENSP00000516418.1:n.-115-70G>C
ENST00000225512.6:c.81-70G>C (WNT3) MANE Select	ENSP00000225512.5:n.81-70G>C
ENST00000225512.5:c.81-70G>C (WNT3)	ENSP00000225512.5:n.81-70G>C
ENST00000573788.5:n.492-70G>C (WNT3)
NM_030753.4:c.81-70G>C (WNT3)	NP_110380.1:n.81-70G>C
XM_024450773.1:c.4809+223460C>G (LRRC37A2)	XP_024306541.1:n.4809+223460C>G
NM_030753.5:c.81-70G>C (WNT3) MANE Select	NP_110380.1:n.81-70G>C