Canonical Allele Identifier: CA2034902179
Gene: WNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981742C= , CM000674.2:g.48981742C= GRCh38
NC_000012.11:g.49375525C= , CM000674.1:g.49375525C= GRCh37
NC_000012.10:g.47661792C= NCBI36
NG_033141.1:g.8290C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*102C= MANE Select ENSP00000293549.3:n.*102C=
NM_005430.3:c.*102C= NP_005421.1:n.*102C=
NM_005430.4:c.*102C= MANE Select NP_005421.1:n.*102C=