Canonical Allele Identifier: CA384638929
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981580-G-T
MyVariant Identifiers: chr12:g.49375363G>T (hg19) chr12:g.48981580G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981580G>T , CM000674.2:g.48981580G>T GRCh38
NC_000012.11:g.49375363G>T , CM000674.1:g.49375363G>T GRCh37
NC_000012.10:g.47661630G>T NCBI36
NG_033141.1:g.8128G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1053G>T MANE Select ENSP00000293549.3:p.Trp351Cys
ENST00000293549.3:c.1053G>T ENSP00000293549.3:p.Trp351Cys
ENST00000613114.4:c.1020G>T ENSP00000481240.1:p.Trp340Cys
NM_005430.3:c.1053G>T NP_005421.1:p.Trp351Cys
NM_005430.4:c.1053G>T MANE Select NP_005421.1:p.Trp351Cys
Search 100 bp 5'
Search 100 bp 3'