Canonical Allele Identifier: CA479704591
Gene: WNT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.49375246G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981463G>C , CM000674.2:g.48981463G>C GRCh38
NC_000012.11:g.49375246G>C , CM000674.1:g.49375246G>C GRCh37
NC_000012.10:g.47661513G>C NCBI36
NG_033141.1:g.8011G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.936G>C MANE Select ENSP00000293549.3:p.Gly312=
ENST00000293549.3:c.936G>C ENSP00000293549.3:p.Gly312=
ENST00000613114.4:c.903G>C ENSP00000481240.1:p.Gly301=
NM_005430.3:c.936G>C NP_005421.1:p.Gly312=
NM_005430.4:c.936G>C MANE Select NP_005421.1:p.Gly312=