Canonical Allele Identifier: CA1396762266

Gene: GSK3B

Linked Data

• dbSNP Id: rs1576179101

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119891954A>G , CM000665.2:g.119891954A>G	GRCh38
NC_000003.11:g.119610801A>G , CM000665.1:g.119610801A>G	GRCh37
NC_000003.10:g.121093491A>G	NCBI36
NG_012922.1:g.207464T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.813+13801T>C MANE Select	ENSP00000264235.9:n.813+13801T>C
ENST00000316626.6:c.813+13801T>C	ENSP00000324806.5:n.813+13801T>C
ENST00000650344.2:c.813+13801T>C	ENSP00000497956.2:n.813+13801T>C
ENST00000676566.1:n.639+13801T>C
ENST00000676887.1:c.132-15446T>C	ENSP00000502977.1:n.132-15446T>C
ENST00000676948.1:c.154+8604T>C
ENST00000677046.1:c.98+13801T>C
ENST00000677069.1:c.99-11456T>C
ENST00000677362.1:c.107+20750T>C
ENST00000677483.1:c.99-9120T>C
ENST00000677502.1:n.596+13801T>C
ENST00000677648.1:c.99-11444T>C
ENST00000677716.1:c.131+24090T>C	ENSP00000503671.1:n.131+24090T>C
ENST00000677788.1:n.1283-11456T>C
ENST00000677995.1:c.326+13801T>C	ENSP00000504203.1:n.326+13801T>C
ENST00000678013.1:c.98+13801T>C
ENST00000678181.1:c.85-28349T>C	ENSP00000504266.1:n.85-28349T>C
ENST00000678377.1:c.229+13801T>C	ENSP00000503164.1:n.229+13801T>C
ENST00000678439.1:c.813+13801T>C	ENSP00000503868.1:n.813+13801T>C
ENST00000678509.1:c.99-9120T>C
ENST00000678561.1:c.486+13801T>C	ENSP00000503494.1:n.486+13801T>C
ENST00000678754.1:n.99-7572T>C
ENST00000678787.1:c.195-15446T>C
ENST00000679066.1:c.85-15446T>C	ENSP00000503626.1:n.85-15446T>C
ENST00000679188.1:c.112-15446T>C	ENSP00000504252.1:n.112-15446T>C
ENST00000679194.1:c.108-15446T>C
ENST00000679206.1:c.131+24090T>C	ENSP00000502943.1:n.131+24090T>C
ENST00000264235.12:c.813+13801T>C	ENSP00000264235.8:n.813+13801T>C
ENST00000316626.5:c.813+13801T>C	ENSP00000324806.5:n.813+13801T>C
NM_001146156.1:c.813+13801T>C	NP_001139628.1:n.813+13801T>C
NM_002093.3:c.813+13801T>C	NP_002084.2:n.813+13801T>C
XM_006713610.1:c.813+13801T>C	XP_006713673.1:n.813+13801T>C
XM_006713611.1:c.813+13801T>C	XP_006713674.1:n.813+13801T>C
NM_001354596.1:c.813+13801T>C	NP_001341525.1:n.813+13801T>C
XM_006713610.3:c.813+13801T>C	XP_006713673.1:n.813+13801T>C
NM_001146156.2:c.813+13801T>C MANE Select	NP_001139628.1:n.813+13801T>C
NM_001354596.2:c.813+13801T>C	NP_001341525.1:n.813+13801T>C
NM_002093.4:c.813+13801T>C	NP_002084.2:n.813+13801T>C