Canonical Allele Identifier: CA605233439

Gene: WNT1

Linked Data

• dbSNP Id: rs1184476130
• gnomAD v2: 12-49375455-C-T
• gnomAD v4: 12-48981672-C-T
• MyVariant Identifiers: chr12:g.49375455C>T (hg19) ; chr12:g.48981672C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981672C>T , CM000674.2:g.48981672C>T	GRCh38
NC_000012.11:g.49375455C>T , CM000674.1:g.49375455C>T	GRCh37
NC_000012.10:g.47661722C>T	NCBI36
NG_033141.1:g.8220C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.*32C>T MANE Select	ENSP00000293549.3:n.*32C>T
ENST00000293549.3:c.*32C>T	ENSP00000293549.3:n.*32C>T
NM_005430.3:c.*32C>T	NP_005421.1:n.*32C>T
NM_005430.4:c.*32C>T MANE Select	NP_005421.1:n.*32C>T