Canonical Allele Identifier: CA897856301

Gene: GSK3B

Linked Data

• dbSNP Id: rs1239924598
• MyVariant Identifiers: chr3:g.119610705C>T (hg19) ; chr3:g.119891858C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119891858C>T , CM000665.2:g.119891858C>T	GRCh38
NC_000003.11:g.119610705C>T , CM000665.1:g.119610705C>T	GRCh37
NC_000003.10:g.121093395C>T	NCBI36
NG_012922.1:g.207560G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.813+13897G>A MANE Select	ENSP00000264235.9:n.813+13897G>A
ENST00000316626.6:c.813+13897G>A	ENSP00000324806.5:n.813+13897G>A
ENST00000650344.2:c.813+13897G>A	ENSP00000497956.2:n.813+13897G>A
ENST00000676566.1:n.639+13897G>A
ENST00000676887.1:c.132-15350G>A	ENSP00000502977.1:n.132-15350G>A
ENST00000676948.1:c.154+8700G>A
ENST00000677046.1:c.98+13897G>A
ENST00000677069.1:c.99-11360G>A
ENST00000677362.1:c.107+20846G>A
ENST00000677483.1:c.99-9024G>A
ENST00000677502.1:n.596+13897G>A
ENST00000677648.1:c.99-11348G>A
ENST00000677716.1:c.131+24186G>A	ENSP00000503671.1:n.131+24186G>A
ENST00000677788.1:n.1283-11360G>A
ENST00000677995.1:c.326+13897G>A	ENSP00000504203.1:n.326+13897G>A
ENST00000678013.1:c.98+13897G>A
ENST00000678181.1:c.85-28253G>A	ENSP00000504266.1:n.85-28253G>A
ENST00000678377.1:c.229+13897G>A	ENSP00000503164.1:n.229+13897G>A
ENST00000678439.1:c.813+13897G>A	ENSP00000503868.1:n.813+13897G>A
ENST00000678509.1:c.99-9024G>A
ENST00000678561.1:c.486+13897G>A	ENSP00000503494.1:n.486+13897G>A
ENST00000678754.1:n.99-7476G>A
ENST00000678787.1:c.195-15350G>A
ENST00000679066.1:c.85-15350G>A	ENSP00000503626.1:n.85-15350G>A
ENST00000679188.1:c.112-15350G>A	ENSP00000504252.1:n.112-15350G>A
ENST00000679194.1:c.108-15350G>A
ENST00000679206.1:c.131+24186G>A	ENSP00000502943.1:n.131+24186G>A
ENST00000264235.12:c.813+13897G>A	ENSP00000264235.8:n.813+13897G>A
ENST00000316626.5:c.813+13897G>A	ENSP00000324806.5:n.813+13897G>A
NM_001146156.1:c.813+13897G>A	NP_001139628.1:n.813+13897G>A
NM_002093.3:c.813+13897G>A	NP_002084.2:n.813+13897G>A
XM_006713610.1:c.813+13897G>A	XP_006713673.1:n.813+13897G>A
XM_006713611.1:c.813+13897G>A	XP_006713674.1:n.813+13897G>A
NM_001354596.1:c.813+13897G>A	NP_001341525.1:n.813+13897G>A
XM_006713610.3:c.813+13897G>A	XP_006713673.1:n.813+13897G>A
NM_001146156.2:c.813+13897G>A MANE Select	NP_001139628.1:n.813+13897G>A
NM_001354596.2:c.813+13897G>A	NP_001341525.1:n.813+13897G>A
NM_002093.4:c.813+13897G>A	NP_002084.2:n.813+13897G>A