Canonical Allele Identifier: CA15277204
Gene: GSK3B-DT HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.120096110T>A
GRCh37 chr3:g.119814957T>A
gnomAD v2:
3:119814957 T / A
gnomAD v3:
3:120096110 T / A
gnomAD v4:
chr3-120096110-T-A
Joint Max Group AF 0.17383642 (SAS)
Genomes Max Group AF 0.17383642 (SAS)
Exomes Max Group AF 0.01776792 (NFE)
dbSNP:
3755557
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120096110T>A , CM000665.2:g.120096110T>A GRCh38
NC_000003.11:g.119814957T>A , CM000665.1:g.119814957T>A GRCh37
NC_000003.10:g.121297647T>A NCBI36
NG_012922.1:g.3308A>T

Transcript Alleles

HGVS Amino-acid Change
XR_001740863.2:n.79+332T>A
XR_002959638.1:n.280T>A
Search 100 bp 5'
Search 100 bp 3'