Canonical Allele Identifier: CA2618599785
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981656-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981656C>A , CM000674.2:g.48981656C>A GRCh38
NC_000012.11:g.49375439C>A , CM000674.1:g.49375439C>A GRCh37
NC_000012.10:g.47661706C>A NCBI36
NG_033141.1:g.8204C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*16C>A MANE Select ENSP00000293549.3:n.*16C>A
ENST00000293549.3:c.*16C>A ENSP00000293549.3:n.*16C>A
NM_005430.3:c.*16C>A NP_005421.1:n.*16C>A
NM_005430.4:c.*16C>A MANE Select NP_005421.1:n.*16C>A
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