Canonical Allele Identifier: CA437079769

Gene: GNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179401318A>C , CM000665.2:g.179401318A>C	GRCh38
NC_000003.11:g.179119106A>C , CM000665.1:g.179119106A>C	GRCh37
NC_000003.10:g.180601800A>C	NCBI36
NG_033163.1:g.55266T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232564.8:c.918T>G MANE Select	ENSP00000232564.3:p.Gly306=
ENST00000466899.6:c.701T>G	ENSP00000420066.2:p.Val234Gly
ENST00000468623.6:c.879T>G	ENSP00000419693.2:p.Gly293=
ENST00000674713.1:c.810T>G	ENSP00000502144.1:p.Gly270=
ENST00000674862.1:c.918T>G	ENSP00000502628.1:p.Gly306=
ENST00000676128.1:c.918T>G	ENSP00000501882.1:p.Gly306=
ENST00000232564.7:c.918T>G	ENSP00000232564.3:p.Gly306=
ENST00000466899.5:c.468T>G
ENST00000468623.5:c.918T>G	ENSP00000419693.1:p.Gly306=
NM_021629.3:c.918T>G	NP_067642.1:p.Gly306=
XM_005247692.1:c.918T>G	XP_005247749.1:p.Gly306=
XM_006713721.1:c.918T>G	XP_006713784.1:p.Gly306=
XM_005247692.2:c.918T>G	XP_005247749.1:p.Gly306=
XM_006713721.2:c.918T>G	XP_006713784.1:p.Gly306=
NM_021629.4:c.918T>G MANE Select	NP_067642.1:p.Gly306=