Canonical Allele Identifier: CA2667150597

Gene: GSK3B

Linked Data

• gnomAD v4: 3-120094337-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120094337C>G , CM000665.2:g.120094337C>G	GRCh38
NC_000003.11:g.119813184C>G , CM000665.1:g.119813184C>G	GRCh37
NC_000003.10:g.121295874C>G	NCBI36
NG_012922.1:g.5081G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264235.13:c.-903G>C MANE Select	ENSP00000264235.9:n.-903G>C
ENST00000677034.1:c.-903G>C	ENSP00000504055.1:n.-903G>C
ENST00000677338.1:c.-160+629G>C	ENSP00000503497.1:n.-160+629G>C
ENST00000677903.1:c.-160+206G>C	ENSP00000503112.1:n.-160+206G>C
ENST00000264235.12:c.-903G>C	ENSP00000264235.8:n.-903G>C
NM_001146156.1:c.-903G>C	NP_001139628.1:n.-903G>C
NM_002093.3:c.-903G>C	NP_002084.2:n.-903G>C
NM_001354596.1:c.-903G>C	NP_001341525.1:n.-903G>C
XR_002959518.1:n.1487G>C
NM_001146156.2:c.-903G>C MANE Select	NP_001139628.1:n.-903G>C
NM_001354596.2:c.-903G>C	NP_001341525.1:n.-903G>C
NM_002093.4:c.-903G>C	NP_002084.2:n.-903G>C