Canonical Allele Identifier: CA1396853628

Gene: GSK3B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120094344G= , CM000665.2:g.120094344G=	GRCh38
NC_000003.11:g.119813191G= , CM000665.1:g.119813191G=	GRCh37
NC_000003.10:g.121295881G=	NCBI36
NG_012922.1:g.5074C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264235.13:c.-910C= MANE Select	ENSP00000264235.9:n.-910C=
ENST00000677034.1:c.-910C=	ENSP00000504055.1:n.-910C=
ENST00000677338.1:c.-160+622C=	ENSP00000503497.1:n.-160+622C=
ENST00000677903.1:c.-160+199C=	ENSP00000503112.1:n.-160+199C=
ENST00000264235.12:c.-910C=	ENSP00000264235.8:n.-910C=
NM_001146156.1:c.-910C=	NP_001139628.1:n.-910C=
NM_002093.3:c.-910C=	NP_002084.2:n.-910C=
NM_001354596.1:c.-910C=	NP_001341525.1:n.-910C=
XR_002959518.1:n.1480C=
NM_001146156.2:c.-910C= MANE Select	NP_001139628.1:n.-910C=
NM_001354596.2:c.-910C=	NP_001341525.1:n.-910C=
NM_002093.4:c.-910C=	NP_002084.2:n.-910C=