Canonical Allele Identifier: CA355469363

Gene: GNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179413470C>T , CM000665.2:g.179413470C>T	GRCh38
NC_000003.11:g.179131258C>T , CM000665.1:g.179131258C>T	GRCh37
NC_000003.10:g.180613952C>T	NCBI36
NG_033163.1:g.43114G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232564.8:c.641G>A MANE Select	ENSP00000232564.3:p.Arg214Gln
ENST00000465153.2:c.641G>A	ENSP00000502010.1:p.Arg214Gln
ENST00000466899.6:c.641G>A	ENSP00000420066.2:p.Arg214Gln
ENST00000468623.6:c.602G>A	ENSP00000419693.2:p.Arg201Gln
ENST00000674713.1:c.533G>A	ENSP00000502144.1:p.Arg178Gln
ENST00000674862.1:c.641G>A	ENSP00000502628.1:p.Arg214Gln
ENST00000674927.1:c.641G>A	ENSP00000501774.1:p.Arg214Gln
ENST00000675901.1:c.641G>A	ENSP00000501992.1:p.Arg214Gln
ENST00000676128.1:c.641G>A	ENSP00000501882.1:p.Arg214Gln
ENST00000232564.7:c.641G>A	ENSP00000232564.3:p.Arg214Gln
ENST00000465153.1:n.160G>A
ENST00000466899.5:c.408G>A
ENST00000468623.5:c.641G>A	ENSP00000419693.1:p.Arg214Gln
NM_021629.3:c.641G>A	NP_067642.1:p.Arg214Gln
XM_005247692.1:c.641G>A	XP_005247749.1:p.Arg214Gln
XM_006713721.1:c.641G>A	XP_006713784.1:p.Arg214Gln
XM_011513061.1:c.641G>A	XP_011511363.1:p.Arg214Gln
XM_005247692.2:c.641G>A	XP_005247749.1:p.Arg214Gln
XM_006713721.2:c.641G>A	XP_006713784.1:p.Arg214Gln
NM_021629.4:c.641G>A MANE Select	NP_067642.1:p.Arg214Gln