Canonical Allele Identifier: CA1396853625

Gene: GSK3B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120094342C= , CM000665.2:g.120094342C=	GRCh38
NC_000003.11:g.119813189C= , CM000665.1:g.119813189C=	GRCh37
NC_000003.10:g.121295879C=	NCBI36
NG_012922.1:g.5076G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264235.13:c.-908G= MANE Select	ENSP00000264235.9:n.-908G=
ENST00000677034.1:c.-908G=	ENSP00000504055.1:n.-908G=
ENST00000677338.1:c.-160+624G=	ENSP00000503497.1:n.-160+624G=
ENST00000677903.1:c.-160+201G=	ENSP00000503112.1:n.-160+201G=
ENST00000264235.12:c.-908G=	ENSP00000264235.8:n.-908G=
NM_001146156.1:c.-908G=	NP_001139628.1:n.-908G=
NM_002093.3:c.-908G=	NP_002084.2:n.-908G=
NM_001354596.1:c.-908G=	NP_001341525.1:n.-908G=
XR_002959518.1:n.1482G=
NM_001146156.2:c.-908G= MANE Select	NP_001139628.1:n.-908G=
NM_001354596.2:c.-908G=	NP_001341525.1:n.-908G=
NM_002093.4:c.-908G=	NP_002084.2:n.-908G=