Canonical Allele Identifier: CA479704450
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981382-C-A
COSMIC: COSM939945
MyVariant Identifiers: chr12:g.49375165C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981382C>A , CM000674.2:g.48981382C>A GRCh38
NC_000012.11:g.49375165C>A , CM000674.1:g.49375165C>A GRCh37
NC_000012.10:g.47661432C>A NCBI36
NG_033141.1:g.7930C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.855C>A MANE Select ENSP00000293549.3:p.Ser285=
ENST00000293549.3:c.855C>A ENSP00000293549.3:p.Ser285=
ENST00000613114.4:c.828-6C>A ENSP00000481240.1:n.828-6C>A
NM_005430.3:c.855C>A NP_005421.1:p.Ser285=
NM_005430.4:c.855C>A MANE Select NP_005421.1:p.Ser285=
Search 100 bp 5'
Search 100 bp 3'