Canonical Allele Identifier: CA478155686

Gene: GNB3

Linked Data

• gnomAD v4: 12-6842997-C-A
• MyVariant Identifiers: chr12:g.6952161C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6842997C>A , CM000674.2:g.6842997C>A	GRCh38
NC_000012.11:g.6952161C>A , CM000674.1:g.6952161C>A	GRCh37
NC_000012.10:g.6822422C>A	NCBI36
NG_009100.1:g.7787C>A
NG_009100.2:g.7787C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.124C>A MANE Select	ENSP00000229264.3:p.Arg42=
ENST00000229264.7:c.124C>A	ENSP00000229264.3:p.Arg42=
ENST00000435982.6:c.124C>A	ENSP00000414734.2:p.Arg42=
ENST00000537035.1:c.124C>A	ENSP00000445967.1:p.Arg42=
ENST00000539127.5:c.*144C>A	ENSP00000444325.1:n.*144C>A
ENST00000540458.5:n.1475C>A
ENST00000541257.5:c.124C>A	ENSP00000442002.1:p.Arg42=
ENST00000541978.5:c.124C>A	ENSP00000439753.2:p.Arg42=
ENST00000542868.1:n.612C>A
NM_001297571.1:c.124C>A	NP_001284500.1:p.Arg42=
NM_002075.3:c.124C>A	NP_002066.1:p.Arg42=
XM_011520953.1:c.124C>A	XP_011519255.1:p.Arg42=
XM_011520954.1:c.124C>A	XP_011519256.1:p.Arg42=
XM_011520953.3:c.124C>A	XP_011519255.1:p.Arg42=
NM_001297571.2:c.124C>A	NP_001284500.1:p.Arg42=
NM_002075.4:c.124C>A MANE Select	NP_002066.1:p.Arg42=