Canonical Allele Identifier: CA437178067

Gene: GNB4

Linked Data

• gnomAD v4: 3-179420898-C-A
• MyVariant Identifiers: chr3:g.179138686C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179420898C>A , CM000665.2:g.179420898C>A	GRCh38
NC_000003.11:g.179138686C>A , CM000665.1:g.179138686C>A	GRCh37
NC_000003.10:g.180621380C>A	NCBI36
NG_033163.1:g.35686G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000232564.8:c.87G>T MANE Select	ENSP00000232564.3:p.Thr29=
ENST00000465153.2:c.87G>T	ENSP00000502010.1:p.Thr29=
ENST00000466899.6:c.87G>T	ENSP00000420066.2:p.Thr29=
ENST00000468623.6:c.58-1393G>T	ENSP00000419693.2:n.58-1393G>T
ENST00000674713.1:c.-22G>T	ENSP00000502144.1:n.-22G>T
ENST00000674862.1:c.87G>T	ENSP00000502628.1:p.Thr29=
ENST00000674927.1:c.87G>T	ENSP00000501774.1:p.Thr29=
ENST00000675901.1:c.87G>T	ENSP00000501992.1:p.Thr29=
ENST00000676128.1:c.87G>T	ENSP00000501882.1:p.Thr29=
ENST00000232564.7:c.87G>T	ENSP00000232564.3:p.Thr29=
ENST00000468623.5:c.87G>T	ENSP00000419693.1:p.Thr29=
ENST00000497513.1:c.87G>T	ENSP00000420606.1:p.Thr29=
NM_021629.3:c.87G>T	NP_067642.1:p.Thr29=
XM_005247692.1:c.87G>T	XP_005247749.1:p.Thr29=
XM_006713721.1:c.87G>T	XP_006713784.1:p.Thr29=
XM_011513061.1:c.87G>T	XP_011511363.1:p.Thr29=
XM_005247692.2:c.87G>T	XP_005247749.1:p.Thr29=
XM_006713721.2:c.87G>T	XP_006713784.1:p.Thr29=
NM_021629.4:c.87G>T MANE Select	NP_067642.1:p.Thr29=