Canonical Allele Identifier: CA2014278935

Gene: GNB3 CDCA3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6847129C= , CM000674.2:g.6847129C=	GRCh38
NC_000012.11:g.6956293C= , CM000674.1:g.6956293C=	GRCh37
NC_000012.10:g.6826554C=	NCBI36
NG_009100.1:g.11919C=
NG_009100.2:g.11919C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.*231C= (GNB3) MANE Select	ENSP00000229264.3:n.*231C=
ENST00000229264.7:c.*231C= (GNB3)	ENSP00000229264.3:n.*231C=
ENST00000422785.7:c.545-226G= (CDCA3)	ENSP00000415142.2:n.545-226G=
ENST00000540458.5:n.2605C= (GNB3)
ENST00000542751.1:n.774C= (GNB3)
ENST00000603043.1:n.308-226G= (CDCA3)
ENST00000604599.1:n.813-226G= (CDCA3)
NM_001297571.1:c.*231C= (GNB3)	NP_001284500.1:n.*231C=
NM_001297603.1:c.545-226G= (CDCA3)	NP_001284532.1:n.545-226G=
NM_002075.3:c.*231C= (GNB3)	NP_002066.1:n.*231C=
XM_011521027.1:c.*983-226G= (CDCA3)	XP_011519329.1:n.*983-226G=
XM_011521028.1:c.*983-226G= (CDCA3)	XP_011519330.1:n.*983-226G=
XM_011521029.1:c.*1201-226G= (CDCA3)	XP_011519331.1:n.*1201-226G=
XM_011521030.1:c.*1134-226G= (CDCA3)	XP_011519332.1:n.*1134-226G=
NM_001297603.2:c.545-226G= (CDCA3)	NP_001284532.1:n.545-226G=
XR_001748879.2:n.2528-226G= (CDCA3)
XR_001748880.2:n.1879-226G= (CDCA3)
XR_001748881.2:n.1788-226G= (CDCA3)
XR_002957383.1:n.2030-226G= (CDCA3)
XR_002957384.1:n.2941-226G= (CDCA3)
XR_002957385.1:n.2421-226G= (CDCA3)
NM_001297571.2:c.*231C= (GNB3)	NP_001284500.1:n.*231C=
NM_002075.4:c.*231C= (GNB3) MANE Select	NP_002066.1:n.*231C=
NM_001297603.3:c.545-226G= (CDCA3)	NP_001284532.1:n.545-226G=