Canonical Allele Identifier: CA2034902153
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs1592258201
gnomAD v4: 12-48981676-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981676T>A , CM000674.2:g.48981676T>A GRCh38
NC_000012.11:g.49375459T>A , CM000674.1:g.49375459T>A GRCh37
NC_000012.10:g.47661726T>A NCBI36
NG_033141.1:g.8224T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*36T>A MANE Select ENSP00000293549.3:n.*36T>A
ENST00000293549.3:c.*36T>A ENSP00000293549.3:n.*36T>A
NM_005430.3:c.*36T>A NP_005421.1:n.*36T>A
NM_005430.4:c.*36T>A MANE Select NP_005421.1:n.*36T>A
Search 100 bp 5'
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