Canonical Allele Identifier: CA2667150614

Gene: GSK3B

Linked Data

• gnomAD v4: 3-120094347-T-A

Genomic Alleles

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

Transcript Alleles

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