Canonical Allele Identifier: CA392489512

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52128246T>C , CM000677.2:g.52128246T>C	GRCh38
NC_000015.9:g.52420443T>C , CM000677.1:g.52420443T>C	GRCh37
NC_000015.8:g.50207735T>C	NCBI36
NG_052868.1:g.68123A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016194.4:c.864-2A>G MANE Select	NP_057278.2:n.864-2A>G
ENST00000261837.12:c.864-2A>G MANE Select	ENSP00000261837.7:n.864-2A>G
NM_001379343.1:c.582-2A>G	NP_001366272.1:n.582-2A>G
NM_006578.3:c.738-2A>G	NP_006569.1:n.738-2A>G
NM_006578.4:c.738-2A>G	NP_006569.1:n.738-2A>G
NM_016194.3:c.864-2A>G	NP_057278.2:n.864-2A>G
ENST00000261837.11:c.864-2A>G	ENSP00000261837.7:n.864-2A>G
ENST00000358784.11:c.738-2A>G	ENSP00000351635.7:n.738-2A>G
ENST00000396335.8:c.528-2A>G	ENSP00000379626.4:n.528-2A>G
ENST00000557936.5:n.550A>G
ENST00000558519.5:c.361-2A>G	ENSP00000453339.1:n.361-2A>G
ENST00000559348.5:n.1345-2A>G
ENST00000559541.1:n.328-2A>G
ENST00000560085.1:n.28A>G
XM_011521162.1:c.738-2A>G	XP_011519464.1:n.738-2A>G
XM_011521162.3:c.738-2A>G	XP_011519464.1:n.738-2A>G
XM_011521163.1:c.582-2A>G	XP_011519465.1:n.582-2A>G
XM_011521163.3:c.582-2A>G	XP_011519465.1:n.582-2A>G
XM_017021867.2:c.315-2A>G	XP_016877356.1:n.315-2A>G
XR_001751060.2:n.816-2A>G