Canonical Allele Identifier: CA2667150610
Gene: GSK3B HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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