Canonical Allele Identifier: CA2014276956

Gene: GNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6842978T= , CM000674.2:g.6842978T=	GRCh38
NC_000012.11:g.6952142T= , CM000674.1:g.6952142T=	GRCh37
NC_000012.10:g.6822403T=	NCBI36
NG_009100.1:g.7768T=
NG_009100.2:g.7768T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.105T= MANE Select	ENSP00000229264.3:p.Ser35=
ENST00000675241.1:c.105T=	ENSP00000501677.1:p.Ser35=
ENST00000229264.7:c.105T=	ENSP00000229264.3:p.Ser35=
ENST00000435982.6:c.105T=	ENSP00000414734.2:p.Ser35=
ENST00000537035.1:c.105T=	ENSP00000445967.1:p.Ser35=
ENST00000539127.5:c.*125T=	ENSP00000444325.1:n.*125T=
ENST00000540458.5:n.1456T=
ENST00000541257.5:c.105T=	ENSP00000442002.1:p.Ser35=
ENST00000541978.5:c.105T=	ENSP00000439753.2:p.Ser35=
ENST00000542868.1:n.593T=
NM_001297571.1:c.105T=	NP_001284500.1:p.Ser35=
NM_002075.3:c.105T=	NP_002066.1:p.Ser35=
XM_011520953.1:c.105T=	XP_011519255.1:p.Ser35=
XM_011520954.1:c.105T=	XP_011519256.1:p.Ser35=
XM_011520953.3:c.105T=	XP_011519255.1:p.Ser35=
NM_001297571.2:c.105T=	NP_001284500.1:p.Ser35=
NM_002075.4:c.105T= MANE Select	NP_002066.1:p.Ser35=