Canonical Allele Identifier: CA604881790

Gene: WNT1

Linked Data

• dbSNP Id: rs1274464742
• gnomAD v2: 12-49375536-C-G
• gnomAD v3: 12-48981753-C-G
• gnomAD v4: 12-48981753-C-G
• MyVariant Identifiers: chr12:g.49375536C>G (hg19) ; chr12:g.48981753C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981753C>G , CM000674.2:g.48981753C>G	GRCh38
NC_000012.11:g.49375536C>G , CM000674.1:g.49375536C>G	GRCh37
NC_000012.10:g.47661803C>G	NCBI36
NG_033141.1:g.8301C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.*113C>G MANE Select	ENSP00000293549.3:n.*113C>G
NM_005430.3:c.*113C>G	NP_005421.1:n.*113C>G
NM_005430.4:c.*113C>G MANE Select	NP_005421.1:n.*113C>G