Canonical Allele Identifier: CA2177210971

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52153971T= , CM000677.2:g.52153971T=	GRCh38
NC_000015.9:g.52446168T= , CM000677.1:g.52446168T=	GRCh37
NC_000015.8:g.50233460T=	NCBI36
NG_052868.1:g.42398A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261837.12:c.344A= MANE Select	ENSP00000261837.7:p.Lys115=
ENST00000261837.11:c.344A=	ENSP00000261837.7:p.Lys115=
ENST00000358784.11:c.218A=	ENSP00000351635.7:p.Lys73=
ENST00000396335.8:c.218A=	ENSP00000379626.4:p.Lys73=
ENST00000560075.1:n.375A=
ENST00000560116.1:c.218A=	ENSP00000453176.1:p.Lys73=
ENST00000561313.5:c.218A=	ENSP00000454185.1:p.Lys73=
NM_006578.3:c.218A=	NP_006569.1:p.Lys73=
NM_016194.3:c.344A=	NP_057278.2:p.Lys115=
XM_011521162.1:c.218A=	XP_011519464.1:p.Lys73=
XM_011521163.1:c.62A=	XP_011519465.1:p.Lys21=
XM_011521162.3:c.218A=	XP_011519464.1:p.Lys73=
XM_011521163.3:c.62A=	XP_011519465.1:p.Lys21=
XR_001751060.2:n.296A=
NM_006578.4:c.218A=	NP_006569.1:p.Lys73=
NM_016194.4:c.344A= MANE Select	NP_057278.2:p.Lys115=
NM_001379343.1:c.62A=	NP_001366272.1:p.Lys21=