Canonical Allele Identifier: CA545918902

Gene: GSK3B

Linked Data

• dbSNP Id: rs1329115002
• gnomAD v2: 3-119813194-T-C
• gnomAD v3: 3-120094347-T-C
• gnomAD v4: 3-120094347-T-C
• MyVariant Identifiers: chr3:g.119813194T>C (hg19) ; chr3:g.120094347T>C (hg38)

Genomic Alleles

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

Transcript Alleles

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