Canonical Allele Identifier: CA1396853639

Gene: GSK3B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120094347T= , CM000665.2:g.120094347T=	GRCh38
NC_000003.11:g.119813194T= , CM000665.1:g.119813194T=	GRCh37
NC_000003.10:g.121295884T=	NCBI36
NG_012922.1:g.5071A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264235.13:c.-913A= MANE Select	ENSP00000264235.9:n.-913A=
ENST00000677034.1:c.-913A=	ENSP00000504055.1:n.-913A=
ENST00000677338.1:c.-160+619A=	ENSP00000503497.1:n.-160+619A=
ENST00000677903.1:c.-160+196A=	ENSP00000503112.1:n.-160+196A=
ENST00000264235.12:c.-913A=	ENSP00000264235.8:n.-913A=
NM_001146156.1:c.-913A=	NP_001139628.1:n.-913A=
NM_002093.3:c.-913A=	NP_002084.2:n.-913A=
NM_001354596.1:c.-913A=	NP_001341525.1:n.-913A=
XR_002959518.1:n.1477A=
NM_001146156.2:c.-913A= MANE Select	NP_001139628.1:n.-913A=
NM_001354596.2:c.-913A=	NP_001341525.1:n.-913A=
NM_002093.4:c.-913A=	NP_002084.2:n.-913A=