Canonical Allele Identifier: CA2034902191
Gene: WNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981767G= , CM000674.2:g.48981767G= GRCh38
NC_000012.11:g.49375550G= , CM000674.1:g.49375550G= GRCh37
NC_000012.10:g.47661817G= NCBI36
NG_033141.1:g.8315G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*127G= MANE Select ENSP00000293549.3:n.*127G=
NM_005430.3:c.*127G= NP_005421.1:n.*127G=
NM_005430.4:c.*127G= MANE Select NP_005421.1:n.*127G=