Canonical Allele Identifier: CA604881791

Gene: WNT1

Linked Data

• dbSNP Id: rs1292134564
• gnomAD v2: 12-49375550-G-T
• gnomAD v3: 12-48981767-G-T
• gnomAD v4: 12-48981767-G-T
• MyVariant Identifiers: chr12:g.49375550G>T (hg19) ; chr12:g.48981767G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981767G>T , CM000674.2:g.48981767G>T	GRCh38
NC_000012.11:g.49375550G>T , CM000674.1:g.49375550G>T	GRCh37
NC_000012.10:g.47661817G>T	NCBI36
NG_033141.1:g.8315G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.*127G>T MANE Select	ENSP00000293549.3:n.*127G>T
NM_005430.3:c.*127G>T	NP_005421.1:n.*127G>T
NM_005430.4:c.*127G>T MANE Select	NP_005421.1:n.*127G>T