Canonical Allele Identifier: CA479704592
Gene: WNT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.49375399G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981616G>C , CM000674.2:g.48981616G>C GRCh38
NC_000012.11:g.49375399G>C , CM000674.1:g.49375399G>C GRCh37
NC_000012.10:g.47661666G>C NCBI36
NG_033141.1:g.8164G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1089G>C MANE Select ENSP00000293549.3:p.Thr363=
ENST00000293549.3:c.1089G>C ENSP00000293549.3:p.Thr363=
ENST00000613114.4:c.1056G>C ENSP00000481240.1:p.Thr352=
NM_005430.3:c.1089G>C NP_005421.1:p.Thr363=
NM_005430.4:c.1089G>C MANE Select NP_005421.1:p.Thr363=
Search 100 bp 5'
Search 100 bp 3'