Canonical Allele Identifier: CA2177210998

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52153979G= , CM000677.2:g.52153979G=	GRCh38
NC_000015.9:g.52446176G= , CM000677.1:g.52446176G=	GRCh37
NC_000015.8:g.50233468G=	NCBI36
NG_052868.1:g.42390C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261837.12:c.336C= MANE Select	ENSP00000261837.7:p.Asp112=
ENST00000261837.11:c.336C=	ENSP00000261837.7:p.Asp112=
ENST00000358784.11:c.210C=	ENSP00000351635.7:p.Asp70=
ENST00000396335.8:c.210C=	ENSP00000379626.4:p.Asp70=
ENST00000560075.1:n.367C=
ENST00000560116.1:c.210C=	ENSP00000453176.1:p.Asp70=
ENST00000561313.5:c.210C=	ENSP00000454185.1:p.Asp70=
NM_006578.3:c.210C=	NP_006569.1:p.Asp70=
NM_016194.3:c.336C=	NP_057278.2:p.Asp112=
XM_011521162.1:c.210C=	XP_011519464.1:p.Asp70=
XM_011521163.1:c.54C=	XP_011519465.1:p.Asp18=
XM_011521162.3:c.210C=	XP_011519464.1:p.Asp70=
XM_011521163.3:c.54C=	XP_011519465.1:p.Asp18=
XR_001751060.2:n.288C=
NM_006578.4:c.210C=	NP_006569.1:p.Asp70=
NM_016194.4:c.336C= MANE Select	NP_057278.2:p.Asp112=
NM_001379343.1:c.54C=	NP_001366272.1:p.Asp18=