Canonical Allele Identifier: CA7565668

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52135629T>C , CM000677.2:g.52135629T>C	GRCh38
NC_000015.9:g.52427826T>C , CM000677.1:g.52427826T>C	GRCh37
NC_000015.8:g.50215118T>C	NCBI36
NG_052868.1:g.60740A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016194.4:c.755A>G MANE Select	NP_057278.2:p.Asn252Ser
ENST00000261837.12:c.755A>G MANE Select	ENSP00000261837.7:p.Asn252Ser
NM_001379343.1:c.473A>G	NP_001366272.1:p.Asn158Ser
NM_006578.3:c.629A>G	NP_006569.1:p.Asn210Ser
NM_006578.4:c.629A>G	NP_006569.1:p.Asn210Ser
NM_016194.3:c.755A>G	NP_057278.2:p.Asn252Ser
ENST00000261837.11:c.755A>G	ENSP00000261837.7:p.Asn252Ser
ENST00000358784.11:c.629A>G	ENSP00000351635.7:p.Asn210Ser
ENST00000396335.8:c.419A>G	ENSP00000379626.4:p.Asn140Ser
ENST00000558519.5:c.200A>G	ENSP00000453339.1:p.Asn67Ser
ENST00000559348.5:n.1236A>G
ENST00000559541.1:n.219A>G
XM_011521162.1:c.629A>G	XP_011519464.1:p.Asn210Ser
XM_011521162.3:c.629A>G	XP_011519464.1:p.Asn210Ser
XM_011521163.1:c.473A>G	XP_011519465.1:p.Asn158Ser
XM_011521163.3:c.473A>G	XP_011519465.1:p.Asn158Ser
XM_017021867.2:c.206A>G	XP_016877356.1:p.Asn69Ser
XR_001751060.2:n.707A>G