Canonical Allele Identifier: CA2618599772
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981653-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981653A>C , CM000674.2:g.48981653A>C GRCh38
NC_000012.11:g.49375436A>C , CM000674.1:g.49375436A>C GRCh37
NC_000012.10:g.47661703A>C NCBI36
NG_033141.1:g.8201A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*13A>C MANE Select ENSP00000293549.3:n.*13A>C
ENST00000293549.3:c.*13A>C ENSP00000293549.3:n.*13A>C
NM_005430.3:c.*13A>C NP_005421.1:n.*13A>C
NM_005430.4:c.*13A>C MANE Select NP_005421.1:n.*13A>C
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