Canonical Allele Identifier: CA392483689

Gene: GNB5

Linked Data

• MyVariant Identifiers: chr15:g.52446248C>A (hg19) ; chr15:g.52154051C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52154051C>A , CM000677.2:g.52154051C>A	GRCh38
NC_000015.9:g.52446248C>A , CM000677.1:g.52446248C>A	GRCh37
NC_000015.8:g.50233540C>A	NCBI36
NG_052868.1:g.42318G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.264G>T MANE Select	ENSP00000261837.7:p.Glu88Asp
ENST00000261837.11:c.264G>T	ENSP00000261837.7:p.Glu88Asp
ENST00000358784.11:c.138G>T	ENSP00000351635.7:p.Glu46Asp
ENST00000396335.8:c.138G>T	ENSP00000379626.4:p.Glu46Asp
ENST00000560075.1:n.295G>T
ENST00000560116.1:c.138G>T	ENSP00000453176.1:p.Glu46Asp
ENST00000561313.5:c.138G>T	ENSP00000454185.1:p.Glu46Asp
NM_006578.3:c.138G>T	NP_006569.1:p.Glu46Asp
NM_016194.3:c.264G>T	NP_057278.2:p.Glu88Asp
XM_011521162.1:c.138G>T	XP_011519464.1:p.Glu46Asp
XM_011521163.1:c.-19G>T	XP_011519465.1:n.-19G>T
XM_011521162.3:c.138G>T	XP_011519464.1:p.Glu46Asp
XM_011521163.3:c.-19G>T	XP_011519465.1:n.-19G>T
XR_001751060.2:n.216G>T
NM_006578.4:c.138G>T	NP_006569.1:p.Glu46Asp
NM_016194.4:c.264G>T MANE Select	NP_057278.2:p.Glu88Asp
NM_001379343.1:c.-19G>T	NP_001366272.1:n.-19G>T