Canonical Allele Identifier: CA2618599912
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981699-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981699C>T , CM000674.2:g.48981699C>T GRCh38
NC_000012.11:g.49375482C>T , CM000674.1:g.49375482C>T GRCh37
NC_000012.10:g.47661749C>T NCBI36
NG_033141.1:g.8247C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*59C>T MANE Select ENSP00000293549.3:n.*59C>T
NM_005430.3:c.*59C>T NP_005421.1:n.*59C>T
NM_005430.4:c.*59C>T MANE Select NP_005421.1:n.*59C>T
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