Canonical Allele Identifier: CA689545075
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs1331055752
gnomAD v3: 12-48981811-C-A
gnomAD v4: 12-48981811-C-A
MyVariant Identifiers: chr12:g.49375594C>A (hg19) chr12:g.48981811C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981811C>A , CM000674.2:g.48981811C>A GRCh38
NC_000012.11:g.49375594C>A , CM000674.1:g.49375594C>A GRCh37
NC_000012.10:g.47661861C>A NCBI36
NG_033141.1:g.8359C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*171C>A MANE Select ENSP00000293549.3:n.*171C>A
NM_005430.3:c.*171C>A NP_005421.1:n.*171C>A
NM_005430.4:c.*171C>A MANE Select NP_005421.1:n.*171C>A
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