Canonical Allele Identifier: CA6417694

Gene: GNB3 CDCA3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6845780C>T , CM000674.2:g.6845780C>T	GRCh38
NC_000012.11:g.6954944C>T , CM000674.1:g.6954944C>T	GRCh37
NC_000012.10:g.6825205C>T	NCBI36
NG_009100.1:g.10570C>T
NG_009100.2:g.10570C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.894C>T (GNB3) MANE Select	ENSP00000229264.3:p.Asp298=
ENST00000229264.7:c.894C>T (GNB3)	ENSP00000229264.3:p.Asp298=
ENST00000422785.7:c.*1008G>A (CDCA3)	ENSP00000415142.2:n.*1008G>A
ENST00000435982.6:c.891C>T (GNB3)	ENSP00000414734.2:p.Asp297=
ENST00000537035.1:c.771C>T (GNB3)	ENSP00000445967.1:p.Asp257=
ENST00000540458.5:n.2245C>T (GNB3)
ENST00000542751.1:n.414C>T (GNB3)
ENST00000603043.1:n.1074G>A (CDCA3)
ENST00000604599.1:n.1936G>A (CDCA3)
NM_001297571.1:c.891C>T (GNB3)	NP_001284500.1:p.Asp297=
NM_002075.3:c.894C>T (GNB3)	NP_002066.1:p.Asp298=
XM_011520953.1:c.894C>T (GNB3)	XP_011519255.1:p.Asp298=
XM_011520954.1:c.891C>T (GNB3)	XP_011519256.1:p.Asp297=
XM_011521027.1:c.*1749G>A (CDCA3)	XP_011519329.1:n.*1749G>A
XM_011521028.1:c.*1749G>A (CDCA3)	XP_011519330.1:n.*1749G>A
XM_011521029.1:c.*1967G>A (CDCA3)	XP_011519331.1:n.*1967G>A
XM_011521030.1:c.*1900G>A (CDCA3)	XP_011519332.1:n.*1900G>A
XM_011520953.3:c.894C>T (GNB3)	XP_011519255.1:p.Asp298=
XR_001748879.2:n.3294G>A (CDCA3)
XR_001748880.2:n.2645G>A (CDCA3)
XR_001748881.2:n.2554G>A (CDCA3)
XR_002957383.1:n.2796G>A (CDCA3)
XR_002957384.1:n.3707G>A (CDCA3)
XR_002957385.1:n.3187G>A (CDCA3)
NM_001297571.2:c.891C>T (GNB3)	NP_001284500.1:p.Asp297=
NM_002075.4:c.894C>T (GNB3) MANE Select	NP_002066.1:p.Asp298=
NM_001297603.3:c.*1008G>A (CDCA3)	NP_001284532.1:n.*1008G>A