Canonical Allele Identifier: CA490403705

Gene: GNB5

Linked Data

• MyVariant Identifiers: chr15:g.52446212G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52154015G>C , CM000677.2:g.52154015G>C	GRCh38
NC_000015.9:g.52446212G>C , CM000677.1:g.52446212G>C	GRCh37
NC_000015.8:g.50233504G>C	NCBI36
NG_052868.1:g.42354C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.300C>G MANE Select	ENSP00000261837.7:p.Thr100=
ENST00000261837.11:c.300C>G	ENSP00000261837.7:p.Thr100=
ENST00000358784.11:c.174C>G	ENSP00000351635.7:p.Thr58=
ENST00000396335.8:c.174C>G	ENSP00000379626.4:p.Thr58=
ENST00000560075.1:n.331C>G
ENST00000560116.1:c.174C>G	ENSP00000453176.1:p.Thr58=
ENST00000561313.5:c.174C>G	ENSP00000454185.1:p.Thr58=
NM_006578.3:c.174C>G	NP_006569.1:p.Thr58=
NM_016194.3:c.300C>G	NP_057278.2:p.Thr100=
XM_011521162.1:c.174C>G	XP_011519464.1:p.Thr58=
XM_011521163.1:c.18C>G	XP_011519465.1:p.Thr6=
XM_011521162.3:c.174C>G	XP_011519464.1:p.Thr58=
XM_011521163.3:c.18C>G	XP_011519465.1:p.Thr6=
XR_001751060.2:n.252C>G
NM_006578.4:c.174C>G	NP_006569.1:p.Thr58=
NM_016194.4:c.300C>G MANE Select	NP_057278.2:p.Thr100=
NM_001379343.1:c.18C>G	NP_001366272.1:p.Thr6=