Canonical Allele Identifier: CA384638782
Gene: WNT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.49375356T>C (hg19) chr12:g.48981573T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981573T>C , CM000674.2:g.48981573T>C GRCh38
NC_000012.11:g.49375356T>C , CM000674.1:g.49375356T>C GRCh37
NC_000012.10:g.47661623T>C NCBI36
NG_033141.1:g.8121T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1046T>C MANE Select ENSP00000293549.3:p.Phe349Ser
ENST00000293549.3:c.1046T>C ENSP00000293549.3:p.Phe349Ser
ENST00000613114.4:c.1013T>C ENSP00000481240.1:p.Phe338Ser
NM_005430.3:c.1046T>C NP_005421.1:p.Phe349Ser
NM_005430.4:c.1046T>C MANE Select NP_005421.1:p.Phe349Ser
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