Canonical Allele Identifier: CA2667150612

Gene: GSK3B

Linked Data

• gnomAD v4: 3-120094345-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120094345G>T , CM000665.2:g.120094345G>T	GRCh38
NC_000003.11:g.119813192G>T , CM000665.1:g.119813192G>T	GRCh37
NC_000003.10:g.121295882G>T	NCBI36
NG_012922.1:g.5073C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264235.13:c.-911C>A MANE Select	ENSP00000264235.9:n.-911C>A
ENST00000677034.1:c.-911C>A	ENSP00000504055.1:n.-911C>A
ENST00000677338.1:c.-160+621C>A	ENSP00000503497.1:n.-160+621C>A
ENST00000677903.1:c.-160+198C>A	ENSP00000503112.1:n.-160+198C>A
ENST00000264235.12:c.-911C>A	ENSP00000264235.8:n.-911C>A
NM_001146156.1:c.-911C>A	NP_001139628.1:n.-911C>A
NM_002093.3:c.-911C>A	NP_002084.2:n.-911C>A
NM_001354596.1:c.-911C>A	NP_001341525.1:n.-911C>A
XR_002959518.1:n.1479C>A
NM_001146156.2:c.-911C>A MANE Select	NP_001139628.1:n.-911C>A
NM_001354596.2:c.-911C>A	NP_001341525.1:n.-911C>A
NM_002093.4:c.-911C>A	NP_002084.2:n.-911C>A