Canonical Allele Identifier: CA2177210992

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52153978A= , CM000677.2:g.52153978A=	GRCh38
NC_000015.9:g.52446175A= , CM000677.1:g.52446175A=	GRCh37
NC_000015.8:g.50233467A=	NCBI36
NG_052868.1:g.42391T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261837.12:c.337T= MANE Select	ENSP00000261837.7:p.Trp113=
ENST00000261837.11:c.337T=	ENSP00000261837.7:p.Trp113=
ENST00000358784.11:c.211T=	ENSP00000351635.7:p.Trp71=
ENST00000396335.8:c.211T=	ENSP00000379626.4:p.Trp71=
ENST00000560075.1:n.368T=
ENST00000560116.1:c.211T=	ENSP00000453176.1:p.Trp71=
ENST00000561313.5:c.211T=	ENSP00000454185.1:p.Trp71=
NM_006578.3:c.211T=	NP_006569.1:p.Trp71=
NM_016194.3:c.337T=	NP_057278.2:p.Trp113=
XM_011521162.1:c.211T=	XP_011519464.1:p.Trp71=
XM_011521163.1:c.55T=	XP_011519465.1:p.Trp19=
XM_011521162.3:c.211T=	XP_011519464.1:p.Trp71=
XM_011521163.3:c.55T=	XP_011519465.1:p.Trp19=
XR_001751060.2:n.289T=
NM_006578.4:c.211T=	NP_006569.1:p.Trp71=
NM_016194.4:c.337T= MANE Select	NP_057278.2:p.Trp113=
NM_001379343.1:c.55T=	NP_001366272.1:p.Trp19=