Canonical Allele Identifier: CA685849314

Gene: WNT5B

Linked Data

• dbSNP Id: rs1435163515
• gnomAD v3: 12-1633270-C-G
• gnomAD v4: 12-1633270-C-G
• MyVariant Identifiers: chr12:g.1742436C>G (hg19) ; chr12:g.1633270C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1633270C>G , CM000674.2:g.1633270C>G	GRCh38
NC_000012.11:g.1742436C>G , CM000674.1:g.1742436C>G	GRCh37
NC_000012.10:g.1612697C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000397196.7:c.328+365C>G MANE Select	ENSP00000380379.2:n.328+365C>G
ENST00000310594.7:c.328+365C>G	ENSP00000308887.3:n.328+365C>G
ENST00000397196.6:c.328+365C>G	ENSP00000380379.2:n.328+365C>G
ENST00000537031.5:c.328+365C>G	ENSP00000439312.1:n.328+365C>G
ENST00000539198.5:c.328+365C>G	ENSP00000438414.1:n.328+365C>G
ENST00000542408.1:c.328+365C>G	ENSP00000440600.1:n.328+365C>G
ENST00000543071.5:c.328+365C>G	ENSP00000442348.1:n.328+365C>G
ENST00000545811.5:c.328+365C>G	ENSP00000445395.1:n.328+365C>G
NM_030775.2:c.328+365C>G	NP_110402.2:n.328+365C>G
NM_032642.2:c.328+365C>G	NP_116031.1:n.328+365C>G
XM_011521026.1:c.328+365C>G	XP_011519328.1:n.328+365C>G
XM_024449203.1:c.484+365C>G	XP_024304971.1:n.484+365C>G
XM_024449204.1:c.391+365C>G	XP_024304972.1:n.391+365C>G
XM_024449205.1:c.328+365C>G	XP_024304973.1:n.328+365C>G
XM_024449206.1:c.328+365C>G	XP_024304974.1:n.328+365C>G
XM_024449207.1:c.328+365C>G	XP_024304975.1:n.328+365C>G
XM_024449208.1:c.328+365C>G	XP_024304976.1:n.328+365C>G
XM_024449209.1:c.328+365C>G	XP_024304977.1:n.328+365C>G
NM_032642.3:c.328+365C>G MANE Select	NP_116031.1:n.328+365C>G