Canonical Allele Identifier: CA1396780186
Gene: GSK3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119931941T>G , CM000665.2:g.119931941T>G GRCh38
NC_000003.11:g.119650788T>G , CM000665.1:g.119650788T>G GRCh37
NC_000003.10:g.121133478T>G NCBI36
NG_012922.1:g.167477A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264235.13:c.367-8458A>C MANE Select ENSP00000264235.9:n.367-8458A>C
ENST00000316626.6:c.367-8458A>C ENSP00000324806.5:n.367-8458A>C
ENST00000650344.2:c.367-8458A>C ENSP00000497956.2:n.367-8458A>C
ENST00000676566.1:n.193-8458A>C
ENST00000676775.1:c.340-8458A>C
ENST00000677169.1:c.*44-8458A>C ENSP00000503107.1:n.*44-8458A>C
ENST00000677502.1:n.150-8458A>C
ENST00000677788.1:n.836-8458A>C
ENST00000677875.1:c.89-8462A>C ENSP00000504503.1:n.89-8462A>C
ENST00000677878.1:c.195-8458A>C
ENST00000677885.1:c.84+15327A>C ENSP00000504148.1:n.84+15327A>C
ENST00000678181.1:c.84+15327A>C ENSP00000504266.1:n.84+15327A>C
ENST00000678245.1:n.824-8458A>C
ENST00000678350.1:c.448-8458A>C
ENST00000678439.1:c.367-8458A>C ENSP00000503868.1:n.367-8458A>C
ENST00000678561.1:c.40-8458A>C ENSP00000503494.1:n.40-8458A>C
ENST00000678787.1:c.195-55433A>C
ENST00000679066.1:c.84+15327A>C ENSP00000503626.1:n.84+15327A>C
ENST00000264235.12:c.367-8458A>C ENSP00000264235.8:n.367-8458A>C
ENST00000316626.5:c.367-8458A>C ENSP00000324806.5:n.367-8458A>C
NM_001146156.1:c.367-8458A>C NP_001139628.1:n.367-8458A>C
NM_002093.3:c.367-8458A>C NP_002084.2:n.367-8458A>C
XM_006713610.1:c.367-8458A>C XP_006713673.1:n.367-8458A>C
XM_006713611.1:c.367-8458A>C XP_006713674.1:n.367-8458A>C
NM_001354596.1:c.367-8458A>C NP_001341525.1:n.367-8458A>C
XM_006713610.3:c.367-8458A>C XP_006713673.1:n.367-8458A>C
NM_001146156.2:c.367-8458A>C MANE Select NP_001139628.1:n.367-8458A>C
NM_001354596.2:c.367-8458A>C NP_001341525.1:n.367-8458A>C
NM_002093.4:c.367-8458A>C NP_002084.2:n.367-8458A>C