Canonical Allele Identifier: CA82398978

Gene: GSK3B

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119922595A>G , CM000665.2:g.119922595A>G	GRCh38
NC_000003.11:g.119641442A>G , CM000665.1:g.119641442A>G	GRCh37
NC_000003.10:g.121124132A>G	NCBI36
NG_012922.1:g.176823T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.477+778T>C MANE Select	ENSP00000264235.9:n.477+778T>C
ENST00000316626.6:c.477+778T>C	ENSP00000324806.5:n.477+778T>C
ENST00000650344.2:c.477+778T>C	ENSP00000497956.2:n.477+778T>C
ENST00000676566.1:n.303+778T>C
ENST00000676723.1:n.111+778T>C
ENST00000677169.1:c.*154+778T>C	ENSP00000503107.1:n.*154+778T>C
ENST00000677502.1:n.260+778T>C
ENST00000677788.1:n.946+778T>C
ENST00000677804.1:n.111+778T>C
ENST00000677885.1:c.85-6421T>C	ENSP00000504148.1:n.85-6421T>C
ENST00000678181.1:c.84+24673T>C	ENSP00000504266.1:n.84+24673T>C
ENST00000678245.1:n.934+778T>C
ENST00000678439.1:c.477+778T>C	ENSP00000503868.1:n.477+778T>C
ENST00000678561.1:c.150+778T>C	ENSP00000503494.1:n.150+778T>C
ENST00000678787.1:c.195-46087T>C
ENST00000679066.1:c.84+24673T>C	ENSP00000503626.1:n.84+24673T>C
ENST00000679188.1:c.111+778T>C	ENSP00000504252.1:n.111+778T>C
ENST00000264235.12:c.477+778T>C	ENSP00000264235.8:n.477+778T>C
ENST00000316626.5:c.477+778T>C	ENSP00000324806.5:n.477+778T>C
NM_001146156.1:c.477+778T>C	NP_001139628.1:n.477+778T>C
NM_002093.3:c.477+778T>C	NP_002084.2:n.477+778T>C
XM_006713610.1:c.477+778T>C	XP_006713673.1:n.477+778T>C
XM_006713611.1:c.477+778T>C	XP_006713674.1:n.477+778T>C
NM_001354596.1:c.477+778T>C	NP_001341525.1:n.477+778T>C
XM_006713610.3:c.477+778T>C	XP_006713673.1:n.477+778T>C
NM_001146156.2:c.477+778T>C MANE Select	NP_001139628.1:n.477+778T>C
NM_001354596.2:c.477+778T>C	NP_001341525.1:n.477+778T>C
NM_002093.4:c.477+778T>C	NP_002084.2:n.477+778T>C