Canonical Allele Identifier: CA479704540
Gene: WNT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.49375219A>G (hg19)
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Genomic Alleles

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

Transcript Alleles

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