Canonical Allele Identifier: CA392483316

Gene: GNB5

Linked Data

• MyVariant Identifiers: chr15:g.52446210A>T (hg19) ; chr15:g.52154013A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52154013A>T , CM000677.2:g.52154013A>T	GRCh38
NC_000015.9:g.52446210A>T , CM000677.1:g.52446210A>T	GRCh37
NC_000015.8:g.50233502A>T	NCBI36
NG_052868.1:g.42356T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.302T>A MANE Select	ENSP00000261837.7:p.Leu101His
ENST00000261837.11:c.302T>A	ENSP00000261837.7:p.Leu101His
ENST00000358784.11:c.176T>A	ENSP00000351635.7:p.Leu59His
ENST00000396335.8:c.176T>A	ENSP00000379626.4:p.Leu59His
ENST00000560075.1:n.333T>A
ENST00000560116.1:c.176T>A	ENSP00000453176.1:p.Leu59His
ENST00000561313.5:c.176T>A	ENSP00000454185.1:p.Leu59His
NM_006578.3:c.176T>A	NP_006569.1:p.Leu59His
NM_016194.3:c.302T>A	NP_057278.2:p.Leu101His
XM_011521162.1:c.176T>A	XP_011519464.1:p.Leu59His
XM_011521163.1:c.20T>A	XP_011519465.1:p.Leu7His
XM_011521162.3:c.176T>A	XP_011519464.1:p.Leu59His
XM_011521163.3:c.20T>A	XP_011519465.1:p.Leu7His
XR_001751060.2:n.254T>A
NM_006578.4:c.176T>A	NP_006569.1:p.Leu59His
NM_016194.4:c.302T>A MANE Select	NP_057278.2:p.Leu101His
NM_001379343.1:c.20T>A	NP_001366272.1:p.Leu7His