Canonical Allele Identifier: CA897909879

Gene: GSK3B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119841759T>A , CM000665.2:g.119841759T>A	GRCh38
NC_000003.11:g.119560606T>A , CM000665.1:g.119560606T>A	GRCh37
NC_000003.10:g.121043296T>A	NCBI36
NG_012922.1:g.257659A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.1195+1496A>T MANE Select	ENSP00000264235.9:n.1195+1496A>T
ENST00000316626.6:c.1234+1496A>T	ENSP00000324806.5:n.1234+1496A>T
ENST00000650344.2:c.1097-14904A>T	ENSP00000497956.2:n.1097-14904A>T
ENST00000676566.1:n.1021+1496A>T
ENST00000676910.1:c.195+1496A>T	ENSP00000504338.1:n.195+1496A>T
ENST00000677502.1:n.978+1496A>T
ENST00000677959.1:n.99+1496A>T
ENST00000678013.1:c.197+1496A>T
ENST00000678159.1:c.100-897A>T
ENST00000678439.1:c.1195+1496A>T	ENSP00000503868.1:n.1195+1496A>T
ENST00000679068.1:c.100-824A>T
ENST00000679201.1:c.97-14904A>T	ENSP00000502998.1:n.97-14904A>T
ENST00000679206.1:c.132-14904A>T	ENSP00000502943.1:n.132-14904A>T
ENST00000264235.12:c.1195+1496A>T	ENSP00000264235.8:n.1195+1496A>T
ENST00000316626.5:c.1234+1496A>T	ENSP00000324806.5:n.1234+1496A>T
ENST00000473886.1:n.284-14904A>T
ENST00000474830.1:n.355+1496A>T
NM_001146156.1:c.1195+1496A>T	NP_001139628.1:n.1195+1496A>T
NM_002093.3:c.1234+1496A>T	NP_002084.2:n.1234+1496A>T
XM_006713610.1:c.1136-14904A>T	XP_006713673.1:n.1136-14904A>T
XM_006713611.1:c.1097-14904A>T	XP_006713674.1:n.1097-14904A>T
NM_001354596.1:c.1097-14904A>T	NP_001341525.1:n.1097-14904A>T
XM_006713610.3:c.1136-14904A>T	XP_006713673.1:n.1136-14904A>T
NM_001146156.2:c.1195+1496A>T MANE Select	NP_001139628.1:n.1195+1496A>T
NM_001354596.2:c.1097-14904A>T	NP_001341525.1:n.1097-14904A>T
NM_002093.4:c.1234+1496A>T	NP_002084.2:n.1234+1496A>T