Canonical Allele Identifier: CA490403718

Gene: GNB5

Linked Data

• MyVariant Identifiers: chr15:g.52446236C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52154039C>T , CM000677.2:g.52154039C>T	GRCh38
NC_000015.9:g.52446236C>T , CM000677.1:g.52446236C>T	GRCh37
NC_000015.8:g.50233528C>T	NCBI36
NG_052868.1:g.42330G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.276G>A MANE Select	ENSP00000261837.7:p.Gln92=
ENST00000261837.11:c.276G>A	ENSP00000261837.7:p.Gln92=
ENST00000358784.11:c.150G>A	ENSP00000351635.7:p.Gln50=
ENST00000396335.8:c.150G>A	ENSP00000379626.4:p.Gln50=
ENST00000560075.1:n.307G>A
ENST00000560116.1:c.150G>A	ENSP00000453176.1:p.Gln50=
ENST00000561313.5:c.150G>A	ENSP00000454185.1:p.Gln50=
NM_006578.3:c.150G>A	NP_006569.1:p.Gln50=
NM_016194.3:c.276G>A	NP_057278.2:p.Gln92=
XM_011521162.1:c.150G>A	XP_011519464.1:p.Gln50=
XM_011521163.1:c.-7G>A	XP_011519465.1:n.-7G>A
XM_011521162.3:c.150G>A	XP_011519464.1:p.Gln50=
XM_011521163.3:c.-7G>A	XP_011519465.1:n.-7G>A
XR_001751060.2:n.228G>A
NM_006578.4:c.150G>A	NP_006569.1:p.Gln50=
NM_016194.4:c.276G>A MANE Select	NP_057278.2:p.Gln92=
NM_001379343.1:c.-7G>A	NP_001366272.1:n.-7G>A