Canonical Allele Identifier: CA1396853622
Gene: GSK3B HGNC NCBI

Linked Data

dbSNP Id: rs1381228780

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120094339G>C , CM000665.2:g.120094339G>C GRCh38
NC_000003.11:g.119813186G>C , CM000665.1:g.119813186G>C GRCh37
NC_000003.10:g.121295876G>C NCBI36
NG_012922.1:g.5079C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264235.13:c.-905C>G MANE Select ENSP00000264235.9:n.-905C>G
ENST00000677034.1:c.-905C>G ENSP00000504055.1:n.-905C>G
ENST00000677338.1:c.-160+627C>G ENSP00000503497.1:n.-160+627C>G
ENST00000677903.1:c.-160+204C>G ENSP00000503112.1:n.-160+204C>G
ENST00000264235.12:c.-905C>G ENSP00000264235.8:n.-905C>G
NM_001146156.1:c.-905C>G NP_001139628.1:n.-905C>G
NM_002093.3:c.-905C>G NP_002084.2:n.-905C>G
NM_001354596.1:c.-905C>G NP_001341525.1:n.-905C>G
XR_002959518.1:n.1485C>G
NM_001146156.2:c.-905C>G MANE Select NP_001139628.1:n.-905C>G
NM_001354596.2:c.-905C>G NP_001341525.1:n.-905C>G
NM_002093.4:c.-905C>G NP_002084.2:n.-905C>G