Canonical Allele Identifier: CA236608865

Gene: WNT1

Linked Data

• dbSNP Id: rs999821734
• gnomAD v2: 12-49375530-A-T
• gnomAD v3: 12-48981747-A-T
• gnomAD v4: 12-48981747-A-T
• MyVariant Identifiers: chr12:g.49375530A>T (hg19) ; chr12:g.48981747A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981747A>T , CM000674.2:g.48981747A>T	GRCh38
NC_000012.11:g.49375530A>T , CM000674.1:g.49375530A>T	GRCh37
NC_000012.10:g.47661797A>T	NCBI36
NG_033141.1:g.8295A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.*107A>T MANE Select	ENSP00000293549.3:n.*107A>T
NM_005430.3:c.*107A>T	NP_005421.1:n.*107A>T
NM_005430.4:c.*107A>T MANE Select	NP_005421.1:n.*107A>T