Canonical Allele Identifier: CA2618599804
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981659-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981659C>A , CM000674.2:g.48981659C>A GRCh38
NC_000012.11:g.49375442C>A , CM000674.1:g.49375442C>A GRCh37
NC_000012.10:g.47661709C>A NCBI36
NG_033141.1:g.8207C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*19C>A MANE Select ENSP00000293549.3:n.*19C>A
ENST00000293549.3:c.*19C>A ENSP00000293549.3:n.*19C>A
NM_005430.3:c.*19C>A NP_005421.1:n.*19C>A
NM_005430.4:c.*19C>A MANE Select NP_005421.1:n.*19C>A
Search 100 bp 5'
Search 100 bp 3'