Canonical Allele Identifier: CA478156153

Gene: GNB3 CDCA3

Linked Data

• MyVariant Identifiers: chr12:g.6954878G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6845714G>T , CM000674.2:g.6845714G>T	GRCh38
NC_000012.11:g.6954878G>T , CM000674.1:g.6954878G>T	GRCh37
NC_000012.10:g.6825139G>T	NCBI36
NG_009100.1:g.10504G>T
NG_009100.2:g.10504G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000229264.8:c.828G>T (GNB3) MANE Select	ENSP00000229264.3:p.Val276=
ENST00000229264.7:c.828G>T (GNB3)	ENSP00000229264.3:p.Val276=
ENST00000422785.7:c.*1074C>A (CDCA3)	ENSP00000415142.2:n.*1074C>A
ENST00000435982.6:c.825G>T (GNB3)	ENSP00000414734.2:p.Val275=
ENST00000537035.1:c.705G>T (GNB3)	ENSP00000445967.1:p.Val235=
ENST00000540458.5:n.2179G>T (GNB3)
ENST00000542751.1:n.348G>T (GNB3)
ENST00000603043.1:n.1140C>A (CDCA3)
ENST00000604599.1:n.2002C>A (CDCA3)
NM_001297571.1:c.825G>T (GNB3)	NP_001284500.1:p.Val275=
NM_002075.3:c.828G>T (GNB3)	NP_002066.1:p.Val276=
XM_011520953.1:c.828G>T (GNB3)	XP_011519255.1:p.Val276=
XM_011520954.1:c.825G>T (GNB3)	XP_011519256.1:p.Val275=
XM_011521027.1:c.*1815C>A (CDCA3)	XP_011519329.1:n.*1815C>A
XM_011521028.1:c.*1815C>A (CDCA3)	XP_011519330.1:n.*1815C>A
XM_011521029.1:c.*2033C>A (CDCA3)	XP_011519331.1:n.*2033C>A
XM_011521030.1:c.*1966C>A (CDCA3)	XP_011519332.1:n.*1966C>A
XM_011520953.3:c.828G>T (GNB3)	XP_011519255.1:p.Val276=
XR_001748879.2:n.3360C>A (CDCA3)
XR_001748880.2:n.2711C>A (CDCA3)
XR_001748881.2:n.2620C>A (CDCA3)
XR_002957383.1:n.2862C>A (CDCA3)
XR_002957384.1:n.3773C>A (CDCA3)
XR_002957385.1:n.3253C>A (CDCA3)
NM_001297571.2:c.825G>T (GNB3)	NP_001284500.1:p.Val275=
NM_002075.4:c.828G>T (GNB3) MANE Select	NP_002066.1:p.Val276=
NM_001297603.3:c.*1074C>A (CDCA3)	NP_001284532.1:n.*1074C>A