Canonical Allele Identifier: CA2618599952
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981716-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981716C>G , CM000674.2:g.48981716C>G GRCh38
NC_000012.11:g.49375499C>G , CM000674.1:g.49375499C>G GRCh37
NC_000012.10:g.47661766C>G NCBI36
NG_033141.1:g.8264C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*76C>G MANE Select ENSP00000293549.3:n.*76C>G
NM_005430.3:c.*76C>G NP_005421.1:n.*76C>G
NM_005430.4:c.*76C>G MANE Select NP_005421.1:n.*76C>G
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