Canonical Allele Identifier: CA2618600198
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981789-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981789T>A , CM000674.2:g.48981789T>A GRCh38
NC_000012.11:g.49375572T>A , CM000674.1:g.49375572T>A GRCh37
NC_000012.10:g.47661839T>A NCBI36
NG_033141.1:g.8337T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*149T>A MANE Select ENSP00000293549.3:n.*149T>A
NM_005430.3:c.*149T>A NP_005421.1:n.*149T>A
NM_005430.4:c.*149T>A MANE Select NP_005421.1:n.*149T>A
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