Canonical Allele Identifier: CA236608879
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs964602627
gnomAD v2: 12-49375587-C-T
gnomAD v3: 12-48981804-C-T
gnomAD v4: 12-48981804-C-T
MyVariant Identifiers: chr12:g.49375587C>T (hg19) chr12:g.48981804C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981804C>T , CM000674.2:g.48981804C>T GRCh38
NC_000012.11:g.49375587C>T , CM000674.1:g.49375587C>T GRCh37
NC_000012.10:g.47661854C>T NCBI36
NG_033141.1:g.8352C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*164C>T MANE Select ENSP00000293549.3:n.*164C>T
NM_005430.3:c.*164C>T NP_005421.1:n.*164C>T
NM_005430.4:c.*164C>T MANE Select NP_005421.1:n.*164C>T
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