Canonical Allele Identifier: CA392483489

Gene: GNB5

Linked Data

• dbSNP Id: rs2034156351
• MyVariant Identifiers: chr15:g.52446228A>G (hg19) ; chr15:g.52154031A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52154031A>G , CM000677.2:g.52154031A>G	GRCh38
NC_000015.9:g.52446228A>G , CM000677.1:g.52446228A>G	GRCh37
NC_000015.8:g.50233520A>G	NCBI36
NG_052868.1:g.42338T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.284T>C MANE Select	ENSP00000261837.7:p.Met95Thr
ENST00000261837.11:c.284T>C	ENSP00000261837.7:p.Met95Thr
ENST00000358784.11:c.158T>C	ENSP00000351635.7:p.Met53Thr
ENST00000396335.8:c.158T>C	ENSP00000379626.4:p.Met53Thr
ENST00000560075.1:n.315T>C
ENST00000560116.1:c.158T>C	ENSP00000453176.1:p.Met53Thr
ENST00000561313.5:c.158T>C	ENSP00000454185.1:p.Met53Thr
NM_006578.3:c.158T>C	NP_006569.1:p.Met53Thr
NM_016194.3:c.284T>C	NP_057278.2:p.Met95Thr
XM_011521162.1:c.158T>C	XP_011519464.1:p.Met53Thr
XM_011521163.1:c.2T>C	XP_011519465.1:p.Met1Thr
XM_011521162.3:c.158T>C	XP_011519464.1:p.Met53Thr
XM_011521163.3:c.2T>C	XP_011519465.1:p.Met1Thr
XR_001751060.2:n.236T>C
NM_006578.4:c.158T>C	NP_006569.1:p.Met53Thr
NM_016194.4:c.284T>C MANE Select	NP_057278.2:p.Met95Thr
NM_001379343.1:c.2T>C	NP_001366272.1:p.Met1Thr