Canonical Allele Identifier: CA2034902186
Gene: WNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981758G= , CM000674.2:g.48981758G= GRCh38
NC_000012.11:g.49375541G= , CM000674.1:g.49375541G= GRCh37
NC_000012.10:g.47661808G= NCBI36
NG_033141.1:g.8306G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*118G= MANE Select ENSP00000293549.3:n.*118G=
NM_005430.3:c.*118G= NP_005421.1:n.*118G=
NM_005430.4:c.*118G= MANE Select NP_005421.1:n.*118G=