Canonical Allele Identifier: CA479704440
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981535-G-A
MyVariant Identifiers: chr12:g.49375318G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981535G>A , CM000674.2:g.48981535G>A GRCh38
NC_000012.11:g.49375318G>A , CM000674.1:g.49375318G>A GRCh37
NC_000012.10:g.47661585G>A NCBI36
NG_033141.1:g.8083G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1008G>A MANE Select ENSP00000293549.3:p.Thr336=
ENST00000293549.3:c.1008G>A ENSP00000293549.3:p.Thr336=
ENST00000613114.4:c.975G>A ENSP00000481240.1:p.Thr325=
NM_005430.3:c.1008G>A NP_005421.1:p.Thr336=
NM_005430.4:c.1008G>A MANE Select NP_005421.1:p.Thr336=
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