Canonical Allele Identifier: CA479704561
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs1941016355
gnomAD v3: 12-48981601-C-A
gnomAD v4: 12-48981601-C-A
MyVariant Identifiers: chr12:g.49375384C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981601C>A , CM000674.2:g.48981601C>A GRCh38
NC_000012.11:g.49375384C>A , CM000674.1:g.49375384C>A GRCh37
NC_000012.10:g.47661651C>A NCBI36
NG_033141.1:g.8149C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1074C>A MANE Select ENSP00000293549.3:p.Arg358=
ENST00000293549.3:c.1074C>A ENSP00000293549.3:p.Arg358=
ENST00000613114.4:c.1041C>A ENSP00000481240.1:p.Arg347=
NM_005430.3:c.1074C>A NP_005421.1:p.Arg358=
NM_005430.4:c.1074C>A MANE Select NP_005421.1:p.Arg358=
Search 100 bp 5'
Search 100 bp 3'