Canonical Allele Identifier: CA605233443
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs1464855450
gnomAD v2: 12-49375461-G-A
gnomAD v3: 12-48981678-G-A
gnomAD v4: 12-48981678-G-A
MyVariant Identifiers: chr12:g.49375461G>A (hg19) chr12:g.48981678G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981678G>A , CM000674.2:g.48981678G>A GRCh38
NC_000012.11:g.49375461G>A , CM000674.1:g.49375461G>A GRCh37
NC_000012.10:g.47661728G>A NCBI36
NG_033141.1:g.8226G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*38G>A MANE Select ENSP00000293549.3:n.*38G>A
NM_005430.3:c.*38G>A NP_005421.1:n.*38G>A
NM_005430.4:c.*38G>A MANE Select NP_005421.1:n.*38G>A
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