Canonical Allele Identifier: CA82398274

Gene: GSK3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119916546C>G , CM000665.2:g.119916546C>G	GRCh38
NC_000003.11:g.119635393C>G , CM000665.1:g.119635393C>G	GRCh37
NC_000003.10:g.121118083C>G	NCBI36
NG_012922.1:g.182872G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.478-372G>C MANE Select	ENSP00000264235.9:n.478-372G>C
ENST00000316626.6:c.478-372G>C	ENSP00000324806.5:n.478-372G>C
ENST00000650344.2:c.478-372G>C	ENSP00000497956.2:n.478-372G>C
ENST00000676566.1:n.304-372G>C
ENST00000677169.1:c.*155-372G>C	ENSP00000503107.1:n.*155-372G>C
ENST00000677502.1:n.261-372G>C
ENST00000677788.1:n.947-372G>C
ENST00000677885.1:c.85-372G>C	ENSP00000504148.1:n.85-372G>C
ENST00000678181.1:c.84+30722G>C	ENSP00000504266.1:n.84+30722G>C
ENST00000678245.1:n.935-372G>C
ENST00000678439.1:c.478-372G>C	ENSP00000503868.1:n.478-372G>C
ENST00000678561.1:c.151-372G>C	ENSP00000503494.1:n.151-372G>C
ENST00000678787.1:c.195-40038G>C
ENST00000679066.1:c.84+30722G>C	ENSP00000503626.1:n.84+30722G>C
ENST00000679188.1:c.111+6827G>C	ENSP00000504252.1:n.111+6827G>C
ENST00000264235.12:c.478-372G>C	ENSP00000264235.8:n.478-372G>C
ENST00000316626.5:c.478-372G>C	ENSP00000324806.5:n.478-372G>C
NM_001146156.1:c.478-372G>C	NP_001139628.1:n.478-372G>C
NM_002093.3:c.478-372G>C	NP_002084.2:n.478-372G>C
XM_006713610.1:c.478-372G>C	XP_006713673.1:n.478-372G>C
XM_006713611.1:c.478-372G>C	XP_006713674.1:n.478-372G>C
NM_001354596.1:c.478-372G>C	NP_001341525.1:n.478-372G>C
XM_006713610.3:c.478-372G>C	XP_006713673.1:n.478-372G>C
NM_001146156.2:c.478-372G>C MANE Select	NP_001139628.1:n.478-372G>C
NM_001354596.2:c.478-372G>C	NP_001341525.1:n.478-372G>C
NM_002093.4:c.478-372G>C	NP_002084.2:n.478-372G>C