Canonical Allele Identifier: CA2014276996

Gene: GNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6843050C= , CM000674.2:g.6843050C=	GRCh38
NC_000012.11:g.6952214C= , CM000674.1:g.6952214C=	GRCh37
NC_000012.10:g.6822475C=	NCBI36
NG_009100.1:g.7840C=
NG_009100.2:g.7840C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.177C= MANE Select	ENSP00000229264.3:p.Tyr59=
ENST00000229264.7:c.177C=	ENSP00000229264.3:p.Tyr59=
ENST00000435982.6:c.177C=	ENSP00000414734.2:p.Tyr59=
ENST00000537035.1:c.177C=	ENSP00000445967.1:p.Tyr59=
ENST00000539127.5:c.*197C=	ENSP00000444325.1:n.*197C=
ENST00000540458.5:n.1528C=
ENST00000541257.5:c.177C=	ENSP00000442002.1:p.Tyr59=
ENST00000541978.5:c.177C=	ENSP00000439753.2:p.Tyr59=
NM_001297571.1:c.177C=	NP_001284500.1:p.Tyr59=
NM_002075.3:c.177C=	NP_002066.1:p.Tyr59=
XM_011520953.1:c.177C=	XP_011519255.1:p.Tyr59=
XM_011520954.1:c.177C=	XP_011519256.1:p.Tyr59=
XM_011520953.3:c.177C=	XP_011519255.1:p.Tyr59=
NM_001297571.2:c.177C=	NP_001284500.1:p.Tyr59=
NM_002075.4:c.177C= MANE Select	NP_002066.1:p.Tyr59=