Canonical Allele Identifier: CA15228853

Gene: GSK3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120059642T>C , CM000665.2:g.120059642T>C	GRCh38
NC_000003.11:g.119778489T>C , CM000665.1:g.119778489T>C	GRCh37
NC_000003.10:g.121261179T>C	NCBI36
NG_012922.1:g.39776A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.88+33705A>G MANE Select	ENSP00000264235.9:n.88+33705A>G
ENST00000316626.6:c.88+33705A>G	ENSP00000324806.5:n.88+33705A>G
ENST00000650344.2:c.88+33705A>G	ENSP00000497956.2:n.88+33705A>G
ENST00000677034.1:c.88+33705A>G	ENSP00000504055.1:n.88+33705A>G
ENST00000677128.1:c.92+33701A>G	ENSP00000503177.1:n.92+33701A>G
ENST00000677169.1:c.88+33705A>G	ENSP00000503107.1:n.88+33705A>G
ENST00000677530.1:n.545+33705A>G
ENST00000677788.1:n.557+33705A>G
ENST00000678245.1:n.545+33705A>G
ENST00000678439.1:c.88+33705A>G	ENSP00000503868.1:n.88+33705A>G
ENST00000679131.1:n.30+26694A>G
ENST00000264235.12:c.88+33705A>G	ENSP00000264235.8:n.88+33705A>G
ENST00000316626.5:c.88+33705A>G	ENSP00000324806.5:n.88+33705A>G
NM_001146156.1:c.88+33705A>G	NP_001139628.1:n.88+33705A>G
NM_002093.3:c.88+33705A>G	NP_002084.2:n.88+33705A>G
XM_006713610.1:c.88+33705A>G	XP_006713673.1:n.88+33705A>G
XM_006713611.1:c.88+33705A>G	XP_006713674.1:n.88+33705A>G
NM_001354596.1:c.88+33705A>G	NP_001341525.1:n.88+33705A>G
XM_006713610.3:c.88+33705A>G	XP_006713673.1:n.88+33705A>G
XR_002959518.1:n.2477+33705A>G
NM_001146156.2:c.88+33705A>G MANE Select	NP_001139628.1:n.88+33705A>G
NM_001354596.2:c.88+33705A>G	NP_001341525.1:n.88+33705A>G
NM_002093.4:c.88+33705A>G	NP_002084.2:n.88+33705A>G