Canonical Allele Identifier: CA479704539
Gene: WNT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.49375219A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981436A>C , CM000674.2:g.48981436A>C GRCh38
NC_000012.11:g.49375219A>C , CM000674.1:g.49375219A>C GRCh37
NC_000012.10:g.47661486A>C NCBI36
NG_033141.1:g.7984A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.909A>C MANE Select ENSP00000293549.3:p.Gly303=
ENST00000293549.3:c.909A>C ENSP00000293549.3:p.Gly303=
ENST00000613114.4:c.876A>C ENSP00000481240.1:p.Gly292=
NM_005430.3:c.909A>C NP_005421.1:p.Gly303=
NM_005430.4:c.909A>C MANE Select NP_005421.1:p.Gly303=
Search 100 bp 5'
Search 100 bp 3'