Canonical Allele Identifier: CA7565581

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52126075C>T , CM000677.2:g.52126075C>T	GRCh38
NC_000015.9:g.52418272C>T , CM000677.1:g.52418272C>T	GRCh37
NC_000015.8:g.50205564C>T	NCBI36
NG_052868.1:g.70294G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016194.4:c.913-31G>A MANE Select	NP_057278.2:n.913-31G>A
ENST00000261837.12:c.913-31G>A MANE Select	ENSP00000261837.7:n.913-31G>A
NM_001379343.1:c.631-31G>A	NP_001366272.1:n.631-31G>A
NM_006578.3:c.787-31G>A	NP_006569.1:n.787-31G>A
NM_006578.4:c.787-31G>A	NP_006569.1:n.787-31G>A
NM_016194.3:c.913-31G>A	NP_057278.2:n.913-31G>A
ENST00000261837.11:c.913-31G>A	ENSP00000261837.7:n.913-31G>A
ENST00000358784.11:c.787-31G>A	ENSP00000351635.7:n.787-31G>A
ENST00000396335.8:c.577-31G>A	ENSP00000379626.4:n.577-31G>A
ENST00000557936.5:n.601-31G>A
ENST00000558519.5:c.410-31G>A	ENSP00000453339.1:n.410-31G>A
ENST00000559348.5:n.1394-31G>A
ENST00000559541.1:n.377-31G>A
ENST00000560085.1:n.79-31G>A
XM_011521162.1:c.787-31G>A	XP_011519464.1:n.787-31G>A
XM_011521162.3:c.787-31G>A	XP_011519464.1:n.787-31G>A
XM_011521163.1:c.631-31G>A	XP_011519465.1:n.631-31G>A
XM_011521163.3:c.631-31G>A	XP_011519465.1:n.631-31G>A
XM_017021867.2:c.364-31G>A	XP_016877356.1:n.364-31G>A
XR_001751060.2:n.865-31G>A