Canonical Allele Identifier: CA1423757634
Gene: GNB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179420890T= , CM000665.2:g.179420890T= GRCh38
NC_000003.11:g.179138678T= , CM000665.1:g.179138678T= GRCh37
NC_000003.10:g.180621372T= NCBI36
NG_033163.1:g.35694A=

Transcript Alleles

HGVS Amino-acid change
ENST00000232564.8:c.95A= MANE Select ENSP00000232564.3:p.Gln32=
ENST00000465153.2:c.95A= ENSP00000502010.1:p.Gln32=
ENST00000466899.6:c.95A= ENSP00000420066.2:p.Gln32=
ENST00000468623.6:c.58-1385A= ENSP00000419693.2:n.58-1385A=
ENST00000674713.1:c.-14A= ENSP00000502144.1:n.-14A=
ENST00000674862.1:c.95A= ENSP00000502628.1:p.Gln32=
ENST00000674927.1:c.95A= ENSP00000501774.1:p.Gln32=
ENST00000675901.1:c.95A= ENSP00000501992.1:p.Gln32=
ENST00000676128.1:c.95A= ENSP00000501882.1:p.Gln32=
ENST00000232564.7:c.95A= ENSP00000232564.3:p.Gln32=
ENST00000468623.5:c.95A= ENSP00000419693.1:p.Gln32=
ENST00000497513.1:c.95A= ENSP00000420606.1:p.Gln32=
NM_021629.3:c.95A= NP_067642.1:p.Gln32=
XM_005247692.1:c.95A= XP_005247749.1:p.Gln32=
XM_006713721.1:c.95A= XP_006713784.1:p.Gln32=
XM_011513061.1:c.95A= XP_011511363.1:p.Gln32=
XM_005247692.2:c.95A= XP_005247749.1:p.Gln32=
XM_006713721.2:c.95A= XP_006713784.1:p.Gln32=
NM_021629.4:c.95A= MANE Select NP_067642.1:p.Gln32=