Canonical Allele Identifier: CA2618599763
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981650-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981650C>T , CM000674.2:g.48981650C>T GRCh38
NC_000012.11:g.49375433C>T , CM000674.1:g.49375433C>T GRCh37
NC_000012.10:g.47661700C>T NCBI36
NG_033141.1:g.8198C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*10C>T MANE Select ENSP00000293549.3:n.*10C>T
ENST00000293549.3:c.*10C>T ENSP00000293549.3:n.*10C>T
NM_005430.3:c.*10C>T NP_005421.1:n.*10C>T
NM_005430.4:c.*10C>T MANE Select NP_005421.1:n.*10C>T
Search 100 bp 5'
Search 100 bp 3'