Canonical Allele Identifier: CA605233447
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs1345897711
gnomAD v2: 12-49375479-A-G
gnomAD v3: 12-48981696-A-G
gnomAD v4: 12-48981696-A-G
MyVariant Identifiers: chr12:g.49375479A>G (hg19) chr12:g.48981696A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981696A>G , CM000674.2:g.48981696A>G GRCh38
NC_000012.11:g.49375479A>G , CM000674.1:g.49375479A>G GRCh37
NC_000012.10:g.47661746A>G NCBI36
NG_033141.1:g.8244A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*56A>G MANE Select ENSP00000293549.3:n.*56A>G
NM_005430.3:c.*56A>G NP_005421.1:n.*56A>G
NM_005430.4:c.*56A>G MANE Select NP_005421.1:n.*56A>G
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