Canonical Allele Identifier: CA479704463
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981388-C-T
MyVariant Identifiers: chr12:g.49375171C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981388C>T , CM000674.2:g.48981388C>T GRCh38
NC_000012.11:g.49375171C>T , CM000674.1:g.49375171C>T GRCh37
NC_000012.10:g.47661438C>T NCBI36
NG_033141.1:g.7936C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.861C>T MANE Select ENSP00000293549.3:p.His287=
ENST00000293549.3:c.861C>T ENSP00000293549.3:p.His287=
ENST00000613114.4:c.828C>T ENSP00000481240.1:p.Pro276=
NM_005430.3:c.861C>T NP_005421.1:p.His287=
NM_005430.4:c.861C>T MANE Select NP_005421.1:p.His287=
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