Canonical Allele Identifier: CA11557019

Gene: GSK3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119890313T>C , CM000665.2:g.119890313T>C	GRCh38
NC_000003.11:g.119609160T>C , CM000665.1:g.119609160T>C	GRCh37
NC_000003.10:g.121091850T>C	NCBI36
NG_012922.1:g.209105A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.814-13805A>G MANE Select	ENSP00000264235.9:n.814-13805A>G
ENST00000316626.6:c.814-13805A>G	ENSP00000324806.5:n.814-13805A>G
ENST00000650344.2:c.814-13805A>G	ENSP00000497956.2:n.814-13805A>G
ENST00000676566.1:n.640-13805A>G
ENST00000676887.1:c.132-13805A>G	ENSP00000502977.1:n.132-13805A>G
ENST00000676948.1:c.154+10245A>G
ENST00000677046.1:c.98+15442A>G
ENST00000677069.1:c.99-9815A>G
ENST00000677362.1:c.107+22391A>G
ENST00000677483.1:c.99-7479A>G
ENST00000677502.1:n.597-13805A>G
ENST00000677648.1:c.99-9803A>G
ENST00000677716.1:c.131+25731A>G	ENSP00000503671.1:n.131+25731A>G
ENST00000677788.1:n.1283-9815A>G
ENST00000677995.1:c.327-13805A>G	ENSP00000504203.1:n.327-13805A>G
ENST00000678013.1:c.98+15442A>G
ENST00000678181.1:c.85-26708A>G	ENSP00000504266.1:n.85-26708A>G
ENST00000678377.1:c.230-13805A>G	ENSP00000503164.1:n.230-13805A>G
ENST00000678439.1:c.814-13805A>G	ENSP00000503868.1:n.814-13805A>G
ENST00000678509.1:c.99-7479A>G
ENST00000678561.1:c.486+15442A>G	ENSP00000503494.1:n.486+15442A>G
ENST00000678754.1:n.99-5931A>G
ENST00000678787.1:c.195-13805A>G
ENST00000679066.1:c.85-13805A>G	ENSP00000503626.1:n.85-13805A>G
ENST00000679188.1:c.112-13805A>G	ENSP00000504252.1:n.112-13805A>G
ENST00000679194.1:c.108-13805A>G
ENST00000679206.1:c.131+25731A>G	ENSP00000502943.1:n.131+25731A>G
ENST00000264235.12:c.814-13805A>G	ENSP00000264235.8:n.814-13805A>G
ENST00000316626.5:c.814-13805A>G	ENSP00000324806.5:n.814-13805A>G
NM_001146156.1:c.814-13805A>G	NP_001139628.1:n.814-13805A>G
NM_002093.3:c.814-13805A>G	NP_002084.2:n.814-13805A>G
XM_006713610.1:c.814-13805A>G	XP_006713673.1:n.814-13805A>G
XM_006713611.1:c.814-13805A>G	XP_006713674.1:n.814-13805A>G
NM_001354596.1:c.814-13805A>G	NP_001341525.1:n.814-13805A>G
XM_006713610.3:c.814-13805A>G	XP_006713673.1:n.814-13805A>G
NM_001146156.2:c.814-13805A>G MANE Select	NP_001139628.1:n.814-13805A>G
NM_001354596.2:c.814-13805A>G	NP_001341525.1:n.814-13805A>G
NM_002093.4:c.814-13805A>G	NP_002084.2:n.814-13805A>G