Canonical Allele Identifier: CA10582139

Gene: GNB4

Linked Data

• ClinVar Variation Id: 241390
• ClinVar RCV Id: RCV000230205 ; RCV002401905
• dbSNP Id: rs878855069
• MyVariant Identifiers: chr3:g.179123123T>C (hg19) ; chr3:g.179405335T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179405335T>C , CM000665.2:g.179405335T>C	GRCh38
NC_000003.11:g.179123123T>C , CM000665.1:g.179123123T>C	GRCh37
NC_000003.10:g.180605817T>C	NCBI36
NG_033163.1:g.51249A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232564.8:c.771A>G MANE Select	ENSP00000232564.3:p.Ala257=
ENST00000466899.6:c.700-4016A>G	ENSP00000420066.2:n.700-4016A>G
ENST00000468623.6:c.732A>G	ENSP00000419693.2:p.Ala244=
ENST00000674713.1:c.663A>G	ENSP00000502144.1:p.Ala221=
ENST00000674862.1:c.771A>G	ENSP00000502628.1:p.Ala257=
ENST00000674927.1:c.771A>G	ENSP00000501774.1:p.Ala257=
ENST00000675901.1:c.771A>G	ENSP00000501992.1:p.Ala257=
ENST00000676128.1:c.771A>G	ENSP00000501882.1:p.Ala257=
ENST00000232564.7:c.771A>G	ENSP00000232564.3:p.Ala257=
ENST00000466899.5:c.467-4016A>G
ENST00000468623.5:c.771A>G	ENSP00000419693.1:p.Ala257=
NM_021629.3:c.771A>G	NP_067642.1:p.Ala257=
XM_005247692.1:c.771A>G	XP_005247749.1:p.Ala257=
XM_006713721.1:c.771A>G	XP_006713784.1:p.Ala257=
XM_005247692.2:c.771A>G	XP_005247749.1:p.Ala257=
XM_006713721.2:c.771A>G	XP_006713784.1:p.Ala257=
NM_021629.4:c.771A>G MANE Select	NP_067642.1:p.Ala257=