Canonical Allele Identifier: CA2667150594

Gene: GSK3B

Linked Data

• gnomAD v4: 3-120094336-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120094336G>C , CM000665.2:g.120094336G>C	GRCh38
NC_000003.11:g.119813183G>C , CM000665.1:g.119813183G>C	GRCh37
NC_000003.10:g.121295873G>C	NCBI36
NG_012922.1:g.5082C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264235.13:c.-902C>G MANE Select	ENSP00000264235.9:n.-902C>G
ENST00000677034.1:c.-902C>G	ENSP00000504055.1:n.-902C>G
ENST00000677338.1:c.-160+630C>G	ENSP00000503497.1:n.-160+630C>G
ENST00000677903.1:c.-160+207C>G	ENSP00000503112.1:n.-160+207C>G
ENST00000264235.12:c.-902C>G	ENSP00000264235.8:n.-902C>G
NM_001146156.1:c.-902C>G	NP_001139628.1:n.-902C>G
NM_002093.3:c.-902C>G	NP_002084.2:n.-902C>G
NM_001354596.1:c.-902C>G	NP_001341525.1:n.-902C>G
XR_002959518.1:n.1488C>G
NM_001146156.2:c.-902C>G MANE Select	NP_001139628.1:n.-902C>G
NM_001354596.2:c.-902C>G	NP_001341525.1:n.-902C>G
NM_002093.4:c.-902C>G	NP_002084.2:n.-902C>G