Canonical Allele Identifier: CA2712452

Gene: GNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179413466A>C , CM000665.2:g.179413466A>C	GRCh38
NC_000003.11:g.179131254A>C , CM000665.1:g.179131254A>C	GRCh37
NC_000003.10:g.180613948A>C	NCBI36
NG_033163.1:g.43118T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232564.8:c.645T>G MANE Select	ENSP00000232564.3:p.Asp215Glu
ENST00000465153.2:c.645T>G	ENSP00000502010.1:p.Asp215Glu
ENST00000466899.6:c.645T>G	ENSP00000420066.2:p.Asp215Glu
ENST00000468623.6:c.606T>G	ENSP00000419693.2:p.Asp202Glu
ENST00000674713.1:c.537T>G	ENSP00000502144.1:p.Asp179Glu
ENST00000674862.1:c.645T>G	ENSP00000502628.1:p.Asp215Glu
ENST00000674927.1:c.645T>G	ENSP00000501774.1:p.Asp215Glu
ENST00000675901.1:c.645T>G	ENSP00000501992.1:p.Asp215Glu
ENST00000676128.1:c.645T>G	ENSP00000501882.1:p.Asp215Glu
ENST00000232564.7:c.645T>G	ENSP00000232564.3:p.Asp215Glu
ENST00000465153.1:n.164T>G
ENST00000466899.5:c.412T>G
ENST00000468623.5:c.645T>G	ENSP00000419693.1:p.Asp215Glu
NM_021629.3:c.645T>G	NP_067642.1:p.Asp215Glu
XM_005247692.1:c.645T>G	XP_005247749.1:p.Asp215Glu
XM_006713721.1:c.645T>G	XP_006713784.1:p.Asp215Glu
XM_011513061.1:c.645T>G	XP_011511363.1:p.Asp215Glu
XM_005247692.2:c.645T>G	XP_005247749.1:p.Asp215Glu
XM_006713721.2:c.645T>G	XP_006713784.1:p.Asp215Glu
NM_021629.4:c.645T>G MANE Select	NP_067642.1:p.Asp215Glu