Canonical Allele Identifier: CA2014276999

Gene: GNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6843055T= , CM000674.2:g.6843055T=	GRCh38
NC_000012.11:g.6952219T= , CM000674.1:g.6952219T=	GRCh37
NC_000012.10:g.6822480T=	NCBI36
NG_009100.1:g.7845T=
NG_009100.2:g.7845T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.182T= MANE Select	ENSP00000229264.3:p.Met61=
ENST00000229264.7:c.182T=	ENSP00000229264.3:p.Met61=
ENST00000435982.6:c.182T=	ENSP00000414734.2:p.Met61=
ENST00000537035.1:c.182T=	ENSP00000445967.1:p.Met61=
ENST00000539127.5:c.*202T=	ENSP00000444325.1:n.*202T=
ENST00000540458.5:n.1533T=
ENST00000541257.5:c.182T=	ENSP00000442002.1:p.Met61=
ENST00000541978.5:c.182T=	ENSP00000439753.2:p.Met61=
NM_001297571.1:c.182T=	NP_001284500.1:p.Met61=
NM_002075.3:c.182T=	NP_002066.1:p.Met61=
XM_011520953.1:c.182T=	XP_011519255.1:p.Met61=
XM_011520954.1:c.182T=	XP_011519256.1:p.Met61=
XM_011520953.3:c.182T=	XP_011519255.1:p.Met61=
NM_001297571.2:c.182T=	NP_001284500.1:p.Met61=
NM_002075.4:c.182T= MANE Select	NP_002066.1:p.Met61=