Canonical Allele Identifier: CA2177211076

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52154050C= , CM000677.2:g.52154050C=	GRCh38
NC_000015.9:g.52446247C= , CM000677.1:g.52446247C=	GRCh37
NC_000015.8:g.50233539C=	NCBI36
NG_052868.1:g.42319G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.265G= MANE Select	ENSP00000261837.7:p.Ala89=
ENST00000261837.11:c.265G=	ENSP00000261837.7:p.Ala89=
ENST00000358784.11:c.139G=	ENSP00000351635.7:p.Ala47=
ENST00000396335.8:c.139G=	ENSP00000379626.4:p.Ala47=
ENST00000560075.1:n.296G=
ENST00000560116.1:c.139G=	ENSP00000453176.1:p.Ala47=
ENST00000561313.5:c.139G=	ENSP00000454185.1:p.Ala47=
NM_006578.3:c.139G=	NP_006569.1:p.Ala47=
NM_016194.3:c.265G=	NP_057278.2:p.Ala89=
XM_011521162.1:c.139G=	XP_011519464.1:p.Ala47=
XM_011521163.1:c.-18G=	XP_011519465.1:n.-18G=
XM_011521162.3:c.139G=	XP_011519464.1:p.Ala47=
XM_011521163.3:c.-18G=	XP_011519465.1:n.-18G=
XR_001751060.2:n.217G=
NM_006578.4:c.139G=	NP_006569.1:p.Ala47=
NM_016194.4:c.265G= MANE Select	NP_057278.2:p.Ala89=
NM_001379343.1:c.-18G=	NP_001366272.1:n.-18G=