Canonical Allele Identifier: CA384639065
Gene: WNT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.49375372C>G (hg19) chr12:g.48981589C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981589C>G , CM000674.2:g.48981589C>G GRCh38
NC_000012.11:g.49375372C>G , CM000674.1:g.49375372C>G GRCh37
NC_000012.10:g.47661639C>G NCBI36
NG_033141.1:g.8137C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1062C>G MANE Select ENSP00000293549.3:p.His354Gln
ENST00000293549.3:c.1062C>G ENSP00000293549.3:p.His354Gln
ENST00000613114.4:c.1029C>G ENSP00000481240.1:p.His343Gln
NM_005430.3:c.1062C>G NP_005421.1:p.His354Gln
NM_005430.4:c.1062C>G MANE Select NP_005421.1:p.His354Gln
Search 100 bp 5'
Search 100 bp 3'