Canonical Allele Identifier: CA2014278132

Gene: GNB3 CDCA3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6845387C= , CM000674.2:g.6845387C=	GRCh38
NC_000012.11:g.6954551C= , CM000674.1:g.6954551C=	GRCh37
NC_000012.10:g.6824812C=	NCBI36
NG_009100.1:g.10177C=
NG_009100.2:g.10177C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.700-199C= (GNB3) MANE Select	ENSP00000229264.3:n.700-199C=
ENST00000229264.7:c.700-199C= (GNB3)	ENSP00000229264.3:n.700-199C=
ENST00000422785.7:c.*1401G= (CDCA3)	ENSP00000415142.2:n.*1401G=
ENST00000435982.6:c.697-199C= (GNB3)	ENSP00000414734.2:n.697-199C=
ENST00000537035.1:c.577-199C= (GNB3)	ENSP00000445967.1:n.577-199C=
ENST00000540458.5:n.2051-199C= (GNB3)
ENST00000542751.1:n.21C= (GNB3)
ENST00000603043.1:n.1467G= (CDCA3)
ENST00000604599.1:n.2329G= (CDCA3)
NM_001297571.1:c.697-199C= (GNB3)	NP_001284500.1:n.697-199C=
NM_002075.3:c.700-199C= (GNB3)	NP_002066.1:n.700-199C=
XM_011520953.1:c.700-199C= (GNB3)	XP_011519255.1:n.700-199C=
XM_011520954.1:c.697-199C= (GNB3)	XP_011519256.1:n.697-199C=
XM_011521027.1:c.*2142G= (CDCA3)	XP_011519329.1:n.*2142G=
XM_011521028.1:c.*2142G= (CDCA3)	XP_011519330.1:n.*2142G=
XM_011521029.1:c.*2360G= (CDCA3)	XP_011519331.1:n.*2360G=
XM_011521030.1:c.*2293G= (CDCA3)	XP_011519332.1:n.*2293G=
XM_011520953.3:c.700-199C= (GNB3)	XP_011519255.1:n.700-199C=
XR_001748879.2:n.3687G= (CDCA3)
XR_001748880.2:n.3038G= (CDCA3)
XR_001748881.2:n.2947G= (CDCA3)
XR_002957383.1:n.3189G= (CDCA3)
XR_002957384.1:n.4100G= (CDCA3)
XR_002957385.1:n.3580G= (CDCA3)
NM_001297571.2:c.697-199C= (GNB3)	NP_001284500.1:n.697-199C=
NM_002075.4:c.700-199C= (GNB3) MANE Select	NP_002066.1:n.700-199C=
NM_001297603.3:c.*1401G= (CDCA3)	NP_001284532.1:n.*1401G=