Canonical Allele Identifier: CA2712409

Gene: GNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179405319A>G , CM000665.2:g.179405319A>G	GRCh38
NC_000003.11:g.179123107A>G , CM000665.1:g.179123107A>G	GRCh37
NC_000003.10:g.180605801A>G	NCBI36
NG_033163.1:g.51265T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232564.8:c.787T>C MANE Select	ENSP00000232564.3:p.Leu263=
ENST00000466899.6:c.700-4000T>C	ENSP00000420066.2:n.700-4000T>C
ENST00000468623.6:c.748T>C	ENSP00000419693.2:p.Leu250=
ENST00000674713.1:c.679T>C	ENSP00000502144.1:p.Leu227=
ENST00000674862.1:c.787T>C	ENSP00000502628.1:p.Leu263=
ENST00000674927.1:c.787T>C	ENSP00000501774.1:p.Leu263=
ENST00000675901.1:c.787T>C	ENSP00000501992.1:p.Leu263=
ENST00000676128.1:c.787T>C	ENSP00000501882.1:p.Leu263=
ENST00000232564.7:c.787T>C	ENSP00000232564.3:p.Leu263=
ENST00000466899.5:c.467-4000T>C
ENST00000468623.5:c.787T>C	ENSP00000419693.1:p.Leu263=
NM_021629.3:c.787T>C	NP_067642.1:p.Leu263=
XM_005247692.1:c.787T>C	XP_005247749.1:p.Leu263=
XM_006713721.1:c.787T>C	XP_006713784.1:p.Leu263=
XM_005247692.2:c.787T>C	XP_005247749.1:p.Leu263=
XM_006713721.2:c.787T>C	XP_006713784.1:p.Leu263=
NM_021629.4:c.787T>C MANE Select	NP_067642.1:p.Leu263=