Canonical Allele Identifier: CA392483068

Gene: GNB5

Linked Data

• MyVariant Identifiers: chr15:g.52446189A>C (hg19) ; chr15:g.52153992A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52153992A>C , CM000677.2:g.52153992A>C	GRCh38
NC_000015.9:g.52446189A>C , CM000677.1:g.52446189A>C	GRCh37
NC_000015.8:g.50233481A>C	NCBI36
NG_052868.1:g.42377T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.323T>G MANE Select	ENSP00000261837.7:p.Val108Gly
ENST00000261837.11:c.323T>G	ENSP00000261837.7:p.Val108Gly
ENST00000358784.11:c.197T>G	ENSP00000351635.7:p.Val66Gly
ENST00000396335.8:c.197T>G	ENSP00000379626.4:p.Val66Gly
ENST00000560075.1:n.354T>G
ENST00000560116.1:c.197T>G	ENSP00000453176.1:p.Val66Gly
ENST00000561313.5:c.197T>G	ENSP00000454185.1:p.Val66Gly
NM_006578.3:c.197T>G	NP_006569.1:p.Val66Gly
NM_016194.3:c.323T>G	NP_057278.2:p.Val108Gly
XM_011521162.1:c.197T>G	XP_011519464.1:p.Val66Gly
XM_011521163.1:c.41T>G	XP_011519465.1:p.Val14Gly
XM_011521162.3:c.197T>G	XP_011519464.1:p.Val66Gly
XM_011521163.3:c.41T>G	XP_011519465.1:p.Val14Gly
XR_001751060.2:n.275T>G
NM_006578.4:c.197T>G	NP_006569.1:p.Val66Gly
NM_016194.4:c.323T>G MANE Select	NP_057278.2:p.Val108Gly
NM_001379343.1:c.41T>G	NP_001366272.1:p.Val14Gly