Canonical Allele Identifier: CA2177210855

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52153917G= , CM000677.2:g.52153917G=	GRCh38
NC_000015.9:g.52446114G= , CM000677.1:g.52446114G=	GRCh37
NC_000015.8:g.50233406G=	NCBI36
NG_052868.1:g.42452C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.375+23C= MANE Select	ENSP00000261837.7:n.375+23C=
ENST00000261837.11:c.375+23C=	ENSP00000261837.7:n.375+23C=
ENST00000358784.11:c.249+23C=	ENSP00000351635.7:n.249+23C=
ENST00000396335.8:c.249+23C=	ENSP00000379626.4:n.249+23C=
ENST00000560075.1:n.406+23C=
ENST00000560116.1:c.249+23C=	ENSP00000453176.1:n.249+23C=
ENST00000561313.5:c.249+23C=	ENSP00000454185.1:n.249+23C=
NM_006578.3:c.249+23C=	NP_006569.1:n.249+23C=
NM_016194.3:c.375+23C=	NP_057278.2:n.375+23C=
XM_011521162.1:c.249+23C=	XP_011519464.1:n.249+23C=
XM_011521163.1:c.93+23C=	XP_011519465.1:n.93+23C=
XM_011521162.3:c.249+23C=	XP_011519464.1:n.249+23C=
XM_011521163.3:c.93+23C=	XP_011519465.1:n.93+23C=
XR_001751060.2:n.327+23C=
NM_006578.4:c.249+23C=	NP_006569.1:n.249+23C=
NM_016194.4:c.375+23C= MANE Select	NP_057278.2:n.375+23C=
NM_001379343.1:c.93+23C=	NP_001366272.1:n.93+23C=