Canonical Allele Identifier: CA384639220
Gene: WNT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.49375394C>G (hg19) chr12:g.48981611C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981611C>G , CM000674.2:g.48981611C>G GRCh38
NC_000012.11:g.49375394C>G , CM000674.1:g.49375394C>G GRCh37
NC_000012.10:g.47661661C>G NCBI36
NG_033141.1:g.8159C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1084C>G MANE Select ENSP00000293549.3:p.His362Asp
ENST00000293549.3:c.1084C>G ENSP00000293549.3:p.His362Asp
ENST00000613114.4:c.1051C>G ENSP00000481240.1:p.His351Asp
NM_005430.3:c.1084C>G NP_005421.1:p.His362Asp
NM_005430.4:c.1084C>G MANE Select NP_005421.1:p.His362Asp
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