Canonical Allele Identifier: CA2014278284

Gene: GNB3 CDCA3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6845719T= , CM000674.2:g.6845719T=	GRCh38
NC_000012.11:g.6954883T= , CM000674.1:g.6954883T=	GRCh37
NC_000012.10:g.6825144T=	NCBI36
NG_009100.1:g.10509T=
NG_009100.2:g.10509T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000229264.8:c.833T= (GNB3) MANE Select	ENSP00000229264.3:p.Phe278=
ENST00000229264.7:c.833T= (GNB3)	ENSP00000229264.3:p.Phe278=
ENST00000422785.7:c.*1069A= (CDCA3)	ENSP00000415142.2:n.*1069A=
ENST00000435982.6:c.830T= (GNB3)	ENSP00000414734.2:p.Phe277=
ENST00000537035.1:c.710T= (GNB3)	ENSP00000445967.1:p.Phe237=
ENST00000540458.5:n.2184T= (GNB3)
ENST00000542751.1:n.353T= (GNB3)
ENST00000603043.1:n.1135A= (CDCA3)
ENST00000604599.1:n.1997A= (CDCA3)
NM_001297571.1:c.830T= (GNB3)	NP_001284500.1:p.Phe277=
NM_002075.3:c.833T= (GNB3)	NP_002066.1:p.Phe278=
XM_011520953.1:c.833T= (GNB3)	XP_011519255.1:p.Phe278=
XM_011520954.1:c.830T= (GNB3)	XP_011519256.1:p.Phe277=
XM_011521027.1:c.*1810A= (CDCA3)	XP_011519329.1:n.*1810A=
XM_011521028.1:c.*1810A= (CDCA3)	XP_011519330.1:n.*1810A=
XM_011521029.1:c.*2028A= (CDCA3)	XP_011519331.1:n.*2028A=
XM_011521030.1:c.*1961A= (CDCA3)	XP_011519332.1:n.*1961A=
XM_011520953.3:c.833T= (GNB3)	XP_011519255.1:p.Phe278=
XR_001748879.2:n.3355A= (CDCA3)
XR_001748880.2:n.2706A= (CDCA3)
XR_001748881.2:n.2615A= (CDCA3)
XR_002957383.1:n.2857A= (CDCA3)
XR_002957384.1:n.3768A= (CDCA3)
XR_002957385.1:n.3248A= (CDCA3)
NM_001297571.2:c.830T= (GNB3)	NP_001284500.1:p.Phe277=
NM_002075.4:c.833T= (GNB3) MANE Select	NP_002066.1:p.Phe278=
NM_001297603.3:c.*1069A= (CDCA3)	NP_001284532.1:n.*1069A=