Canonical Allele Identifier: CA270680687

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52127928T>C , CM000677.2:g.52127928T>C	GRCh38
NC_000015.9:g.52420125T>C , CM000677.1:g.52420125T>C	GRCh37
NC_000015.8:g.50207417T>C	NCBI36
NG_052868.1:g.68441A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016194.4:c.912+268A>G MANE Select	NP_057278.2:n.912+268A>G
ENST00000261837.12:c.912+268A>G MANE Select	ENSP00000261837.7:n.912+268A>G
NM_001379343.1:c.630+268A>G	NP_001366272.1:n.630+268A>G
NM_006578.3:c.786+268A>G	NP_006569.1:n.786+268A>G
NM_006578.4:c.786+268A>G	NP_006569.1:n.786+268A>G
NM_016194.3:c.912+268A>G	NP_057278.2:n.912+268A>G
ENST00000261837.11:c.912+268A>G	ENSP00000261837.7:n.912+268A>G
ENST00000358784.11:c.786+268A>G	ENSP00000351635.7:n.786+268A>G
ENST00000396335.8:c.576+268A>G	ENSP00000379626.4:n.576+268A>G
ENST00000557936.5:n.600+268A>G
ENST00000558519.5:c.409+268A>G	ENSP00000453339.1:n.409+268A>G
ENST00000559348.5:n.1393+268A>G
ENST00000559541.1:n.376+268A>G
ENST00000560085.1:n.78+268A>G
XM_011521162.1:c.786+268A>G	XP_011519464.1:n.786+268A>G
XM_011521162.3:c.786+268A>G	XP_011519464.1:n.786+268A>G
XM_011521163.1:c.630+268A>G	XP_011519465.1:n.630+268A>G
XM_011521163.3:c.630+268A>G	XP_011519465.1:n.630+268A>G
XM_017021867.2:c.363+268A>G	XP_016877356.1:n.363+268A>G
XR_001751060.2:n.864+268A>G