Canonical Allele Identifier: CA2577964487

Gene: GNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179416473G>T , CM000665.2:g.179416473G>T	GRCh38
NC_000003.11:g.179134261G>T , CM000665.1:g.179134261G>T	GRCh37
NC_000003.10:g.180616955G>T	NCBI36
NG_033163.1:g.40111C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232564.8:c.267+20C>A MANE Select	ENSP00000232564.3:n.267+20C>A
ENST00000465153.2:c.267+20C>A	ENSP00000502010.1:n.267+20C>A
ENST00000466899.6:c.267+20C>A	ENSP00000420066.2:n.267+20C>A
ENST00000468623.6:c.228+20C>A	ENSP00000419693.2:n.228+20C>A
ENST00000674713.1:c.159+20C>A	ENSP00000502144.1:n.159+20C>A
ENST00000674862.1:c.267+20C>A	ENSP00000502628.1:n.267+20C>A
ENST00000674927.1:c.267+20C>A	ENSP00000501774.1:n.267+20C>A
ENST00000675901.1:c.267+20C>A	ENSP00000501992.1:n.267+20C>A
ENST00000676128.1:c.267+20C>A	ENSP00000501882.1:n.267+20C>A
ENST00000232564.7:c.267+20C>A	ENSP00000232564.3:n.267+20C>A
ENST00000466899.5:c.34+20C>A
ENST00000468623.5:c.267+20C>A	ENSP00000419693.1:n.267+20C>A
NM_021629.3:c.267+20C>A	NP_067642.1:n.267+20C>A
XM_005247692.1:c.267+20C>A	XP_005247749.1:n.267+20C>A
XM_006713721.1:c.267+20C>A	XP_006713784.1:n.267+20C>A
XM_011513061.1:c.267+20C>A	XP_011511363.1:n.267+20C>A
XM_005247692.2:c.267+20C>A	XP_005247749.1:n.267+20C>A
XM_006713721.2:c.267+20C>A	XP_006713784.1:n.267+20C>A
NM_021629.4:c.267+20C>A MANE Select	NP_067642.1:n.267+20C>A