Canonical Allele Identifier: CA236608859

Gene: WNT1

Linked Data

• dbSNP Id: rs767267224
• gnomAD v3: 12-48981717-G-A
• gnomAD v4: 12-48981717-G-A
• MyVariant Identifiers: chr12:g.49375500G>A (hg19) ; chr12:g.48981717G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981717G>A , CM000674.2:g.48981717G>A	GRCh38
NC_000012.11:g.49375500G>A , CM000674.1:g.49375500G>A	GRCh37
NC_000012.10:g.47661767G>A	NCBI36
NG_033141.1:g.8265G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.*77G>A MANE Select	ENSP00000293549.3:n.*77G>A
NM_005430.3:c.*77G>A	NP_005421.1:n.*77G>A
NM_005430.4:c.*77G>A MANE Select	NP_005421.1:n.*77G>A