Canonical Allele Identifier: CA11584427
Gene: GSK3B HGNC NCBI

Linked Data

dbSNP Id: rs6779828
gnomAD v2: 3-119775147-C-T
gnomAD v3: 3-120056300-C-T
gnomAD v4: 3-120056300-C-T
MyVariant Identifiers: chr3:g.119775147C>T (hg19) chr3:g.120056300C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120056300C>T , CM000665.2:g.120056300C>T GRCh38
NC_000003.11:g.119775147C>T , CM000665.1:g.119775147C>T GRCh37
NC_000003.10:g.121257837C>T NCBI36
NG_012922.1:g.43118G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264235.13:c.88+37047G>A MANE Select ENSP00000264235.9:n.88+37047G>A
ENST00000316626.6:c.88+37047G>A ENSP00000324806.5:n.88+37047G>A
ENST00000650344.2:c.88+37047G>A ENSP00000497956.2:n.88+37047G>A
ENST00000677034.1:c.89-34674G>A ENSP00000504055.1:n.89-34674G>A
ENST00000677128.1:c.92+37043G>A ENSP00000503177.1:n.92+37043G>A
ENST00000677169.1:c.88+37047G>A ENSP00000503107.1:n.88+37047G>A
ENST00000677530.1:n.545+37047G>A
ENST00000677788.1:n.557+37047G>A
ENST00000678245.1:n.545+37047G>A
ENST00000678439.1:c.88+37047G>A ENSP00000503868.1:n.88+37047G>A
ENST00000679131.1:n.30+30036G>A
ENST00000264235.12:c.88+37047G>A ENSP00000264235.8:n.88+37047G>A
ENST00000316626.5:c.88+37047G>A ENSP00000324806.5:n.88+37047G>A
NM_001146156.1:c.88+37047G>A NP_001139628.1:n.88+37047G>A
NM_002093.3:c.88+37047G>A NP_002084.2:n.88+37047G>A
XM_006713610.1:c.88+37047G>A XP_006713673.1:n.88+37047G>A
XM_006713611.1:c.88+37047G>A XP_006713674.1:n.88+37047G>A
NM_001354596.1:c.88+37047G>A NP_001341525.1:n.88+37047G>A
XM_006713610.3:c.88+37047G>A XP_006713673.1:n.88+37047G>A
XR_002959518.1:n.2477+37047G>A
NM_001146156.2:c.88+37047G>A MANE Select NP_001139628.1:n.88+37047G>A
NM_001354596.2:c.88+37047G>A NP_001341525.1:n.88+37047G>A
NM_002093.4:c.88+37047G>A NP_002084.2:n.88+37047G>A
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