Canonical Allele Identifier: CA2034902200
Gene: WNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981810A= , CM000674.2:g.48981810A= GRCh38
NC_000012.11:g.49375593A= , CM000674.1:g.49375593A= GRCh37
NC_000012.10:g.47661860A= NCBI36
NG_033141.1:g.8358A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*170A= MANE Select ENSP00000293549.3:n.*170A=
NM_005430.3:c.*170A= NP_005421.1:n.*170A=
NM_005430.4:c.*170A= MANE Select NP_005421.1:n.*170A=