Canonical Allele Identifier: CA236608842
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs79565269
gnomAD v2: 12-49375442-C-T
MyVariant Identifiers: chr12:g.49375442C>T (hg19) chr12:g.48981659C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981659C>T , CM000674.2:g.48981659C>T GRCh38
NC_000012.11:g.49375442C>T , CM000674.1:g.49375442C>T GRCh37
NC_000012.10:g.47661709C>T NCBI36
NG_033141.1:g.8207C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*19C>T MANE Select ENSP00000293549.3:n.*19C>T
ENST00000293549.3:c.*19C>T ENSP00000293549.3:n.*19C>T
NM_005430.3:c.*19C>T NP_005421.1:n.*19C>T
NM_005430.4:c.*19C>T MANE Select NP_005421.1:n.*19C>T
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