Canonical Allele Identifier: CA479704526
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981577-C-T
MyVariant Identifiers: chr12:g.49375360C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981577C>T , CM000674.2:g.48981577C>T GRCh38
NC_000012.11:g.49375360C>T , CM000674.1:g.49375360C>T GRCh37
NC_000012.10:g.47661627C>T NCBI36
NG_033141.1:g.8125C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1050C>T MANE Select ENSP00000293549.3:p.His350=
ENST00000293549.3:c.1050C>T ENSP00000293549.3:p.His350=
ENST00000613114.4:c.1017C>T ENSP00000481240.1:p.His339=
NM_005430.3:c.1050C>T NP_005421.1:p.His350=
NM_005430.4:c.1050C>T MANE Select NP_005421.1:p.His350=
Search 100 bp 5'
Search 100 bp 3'