Canonical Allele Identifier: CA2618599938
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981710-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981710A>G , CM000674.2:g.48981710A>G GRCh38
NC_000012.11:g.49375493A>G , CM000674.1:g.49375493A>G GRCh37
NC_000012.10:g.47661760A>G NCBI36
NG_033141.1:g.8258A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*70A>G MANE Select ENSP00000293549.3:n.*70A>G
NM_005430.3:c.*70A>G NP_005421.1:n.*70A>G
NM_005430.4:c.*70A>G MANE Select NP_005421.1:n.*70A>G
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