Canonical Allele Identifier: CA2712423

Gene: GNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179405382C>T , CM000665.2:g.179405382C>T	GRCh38
NC_000003.11:g.179123170C>T , CM000665.1:g.179123170C>T	GRCh37
NC_000003.10:g.180605864C>T	NCBI36
NG_033163.1:g.51202G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021629.4:c.724G>A MANE Select	NP_067642.1:p.Ala242Thr
ENST00000232564.8:c.724G>A MANE Select	ENSP00000232564.3:p.Ala242Thr
NM_021629.3:c.724G>A	NP_067642.1:p.Ala242Thr
ENST00000232564.7:c.724G>A	ENSP00000232564.3:p.Ala242Thr
ENST00000466899.5:c.467-4063G>A
ENST00000466899.6:c.700-4063G>A	ENSP00000420066.2:n.700-4063G>A
ENST00000468623.5:c.724G>A	ENSP00000419693.1:p.Ala242Thr
ENST00000468623.6:c.685G>A	ENSP00000419693.2:p.Ala229Thr
ENST00000674713.1:c.616G>A	ENSP00000502144.1:p.Ala206Thr
ENST00000674862.1:c.724G>A	ENSP00000502628.1:p.Ala242Thr
ENST00000674927.1:c.724G>A	ENSP00000501774.1:p.Ala242Thr
ENST00000675901.1:c.724G>A	ENSP00000501992.1:p.Ala242Thr
ENST00000676128.1:c.724G>A	ENSP00000501882.1:p.Ala242Thr
XM_005247692.1:c.724G>A	XP_005247749.1:p.Ala242Thr
XM_005247692.2:c.724G>A	XP_005247749.1:p.Ala242Thr
XM_006713721.1:c.724G>A	XP_006713784.1:p.Ala242Thr
XM_006713721.2:c.724G>A	XP_006713784.1:p.Ala242Thr