Canonical Allele Identifier: CA478155791

Gene: GNB3

Linked Data

• MyVariant Identifiers: chr12:g.6952229C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6843065C>G , CM000674.2:g.6843065C>G	GRCh38
NC_000012.11:g.6952229C>G , CM000674.1:g.6952229C>G	GRCh37
NC_000012.10:g.6822490C>G	NCBI36
NG_009100.1:g.7855C>G
NG_009100.2:g.7855C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.192C>G MANE Select	ENSP00000229264.3:p.Ala64=
ENST00000229264.7:c.192C>G	ENSP00000229264.3:p.Ala64=
ENST00000435982.6:c.192C>G	ENSP00000414734.2:p.Ala64=
ENST00000537035.1:c.192C>G	ENSP00000445967.1:p.Ala64=
ENST00000539127.5:c.*212C>G	ENSP00000444325.1:n.*212C>G
ENST00000540458.5:n.1543C>G
ENST00000541257.5:c.192C>G	ENSP00000442002.1:p.Ala64=
ENST00000541978.5:c.192C>G	ENSP00000439753.2:p.Ala64=
NM_001297571.1:c.192C>G	NP_001284500.1:p.Ala64=
NM_002075.3:c.192C>G	NP_002066.1:p.Ala64=
XM_011520953.1:c.192C>G	XP_011519255.1:p.Ala64=
XM_011520954.1:c.192C>G	XP_011519256.1:p.Ala64=
XM_011520953.3:c.192C>G	XP_011519255.1:p.Ala64=
NM_001297571.2:c.192C>G	NP_001284500.1:p.Ala64=
NM_002075.4:c.192C>G MANE Select	NP_002066.1:p.Ala64=