Canonical Allele Identifier: CA1423757421

Gene: GNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179420690A= , CM000665.2:g.179420690A=	GRCh38
NC_000003.11:g.179138478A= , CM000665.1:g.179138478A=	GRCh37
NC_000003.10:g.180621172A=	NCBI36
NG_033163.1:g.35894T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232564.8:c.96+199T= MANE Select	ENSP00000232564.3:n.96+199T=
ENST00000465153.2:c.96+199T=	ENSP00000502010.1:n.96+199T=
ENST00000466899.6:c.96+199T=	ENSP00000420066.2:n.96+199T=
ENST00000468623.6:c.58-1185T=	ENSP00000419693.2:n.58-1185T=
ENST00000674713.1:c.-13+199T=	ENSP00000502144.1:n.-13+199T=
ENST00000674862.1:c.96+199T=	ENSP00000502628.1:n.96+199T=
ENST00000674927.1:c.96+199T=	ENSP00000501774.1:n.96+199T=
ENST00000675901.1:c.96+199T=	ENSP00000501992.1:n.96+199T=
ENST00000676128.1:c.96+199T=	ENSP00000501882.1:n.96+199T=
ENST00000232564.7:c.96+199T=	ENSP00000232564.3:n.96+199T=
ENST00000468623.5:c.96+199T=	ENSP00000419693.1:n.96+199T=
ENST00000497513.1:c.96+199T=	ENSP00000420606.1:n.96+199T=
NM_021629.3:c.96+199T=	NP_067642.1:n.96+199T=
XM_005247692.1:c.96+199T=	XP_005247749.1:n.96+199T=
XM_006713721.1:c.96+199T=	XP_006713784.1:n.96+199T=
XM_011513061.1:c.96+199T=	XP_011511363.1:n.96+199T=
XM_005247692.2:c.96+199T=	XP_005247749.1:n.96+199T=
XM_006713721.2:c.96+199T=	XP_006713784.1:n.96+199T=
NM_021629.4:c.96+199T= MANE Select	NP_067642.1:n.96+199T=