Canonical Allele Identifier: CA384639467
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981640-A-G
MyVariant Identifiers: chr12:g.49375423A>G (hg19) chr12:g.48981640A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981640A>G , CM000674.2:g.48981640A>G GRCh38
NC_000012.11:g.49375423A>G , CM000674.1:g.49375423A>G GRCh37
NC_000012.10:g.47661690A>G NCBI36
NG_033141.1:g.8188A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1113A>G MANE Select ENSP00000293549.3:p.Ter371Trp
ENST00000293549.3:c.1113A>G ENSP00000293549.3:p.Ter371Trp
ENST00000613114.4:c.1080A>G ENSP00000481240.1:p.Ter360Trp
NM_005430.3:c.1113A>G NP_005421.1:p.Ter371Trp
NM_005430.4:c.1113A>G MANE Select NP_005421.1:p.Ter371Trp
Search 100 bp 5'
Search 100 bp 3'