Canonical Allele Identifier: CA605233446
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs1337150926
gnomAD v2: 12-49375472-C-A
gnomAD v3: 12-48981689-C-A
gnomAD v4: 12-48981689-C-A
MyVariant Identifiers: chr12:g.49375472C>A (hg19) chr12:g.48981689C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981689C>A , CM000674.2:g.48981689C>A GRCh38
NC_000012.11:g.49375472C>A , CM000674.1:g.49375472C>A GRCh37
NC_000012.10:g.47661739C>A NCBI36
NG_033141.1:g.8237C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*49C>A MANE Select ENSP00000293549.3:n.*49C>A
NM_005430.3:c.*49C>A NP_005421.1:n.*49C>A
NM_005430.4:c.*49C>A MANE Select NP_005421.1:n.*49C>A
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