Canonical Allele Identifier: CA2617346633

Gene: GNB3

Linked Data

• gnomAD v4: 12-6843060-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6843063dup , CM000674.2:g.6843063dup	GRCh38
NC_000012.11:g.6952227dup , CM000674.1:g.6952227dup	GRCh37
NC_000012.10:g.6822488dup	NCBI36
NG_009100.1:g.7853dup
NG_009100.2:g.7853dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.190dup MANE Select	ENSP00000229264.3:p.Ala64GlyfsTer3
ENST00000229264.7:c.190dup	ENSP00000229264.3:p.Ala64GlyfsTer3
ENST00000435982.6:c.190dup	ENSP00000414734.2:p.Ala64GlyfsTer3
ENST00000537035.1:c.190dup	ENSP00000445967.1:p.Ala64GlyfsTer3
ENST00000539127.5:c.*210dup	ENSP00000444325.1:n.*210dup
ENST00000540458.5:n.1541dup
ENST00000541257.5:c.190dup	ENSP00000442002.1:p.Ala64GlyfsTer3
ENST00000541978.5:c.190dup	ENSP00000439753.2:p.Ala64GlyfsTer3
NM_001297571.1:c.190dup	NP_001284500.1:p.Ala64GlyfsTer3
NM_002075.3:c.190dup	NP_002066.1:p.Ala64GlyfsTer3
XM_011520953.1:c.190dup	XP_011519255.1:p.Ala64GlyfsTer3
XM_011520954.1:c.190dup	XP_011519256.1:p.Ala64GlyfsTer3
XM_011520953.3:c.190dup	XP_011519255.1:p.Ala64GlyfsTer3
NM_001297571.2:c.190dup	NP_001284500.1:p.Ala64GlyfsTer3
NM_002075.4:c.190dup MANE Select	NP_002066.1:p.Ala64GlyfsTer3