Canonical Allele Identifier: CA2617351372

Gene: GNB3 CDCA3

Linked Data

• gnomAD v4: 12-6845409-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6845409C>A , CM000674.2:g.6845409C>A	GRCh38
NC_000012.11:g.6954573C>A , CM000674.1:g.6954573C>A	GRCh37
NC_000012.10:g.6824834C>A	NCBI36
NG_009100.1:g.10199C>A
NG_009100.2:g.10199C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.700-177C>A (GNB3) MANE Select	ENSP00000229264.3:n.700-177C>A
ENST00000229264.7:c.700-177C>A (GNB3)	ENSP00000229264.3:n.700-177C>A
ENST00000422785.7:c.*1379G>T (CDCA3)	ENSP00000415142.2:n.*1379G>T
ENST00000435982.6:c.697-177C>A (GNB3)	ENSP00000414734.2:n.697-177C>A
ENST00000537035.1:c.577-177C>A (GNB3)	ENSP00000445967.1:n.577-177C>A
ENST00000540458.5:n.2051-177C>A (GNB3)
ENST00000542751.1:n.43C>A (GNB3)
ENST00000603043.1:n.1445G>T (CDCA3)
ENST00000604599.1:n.2307G>T (CDCA3)
NM_001297571.1:c.697-177C>A (GNB3)	NP_001284500.1:n.697-177C>A
NM_002075.3:c.700-177C>A (GNB3)	NP_002066.1:n.700-177C>A
XM_011520953.1:c.700-177C>A (GNB3)	XP_011519255.1:n.700-177C>A
XM_011520954.1:c.697-177C>A (GNB3)	XP_011519256.1:n.697-177C>A
XM_011521027.1:c.*2120G>T (CDCA3)	XP_011519329.1:n.*2120G>T
XM_011521028.1:c.*2120G>T (CDCA3)	XP_011519330.1:n.*2120G>T
XM_011521029.1:c.*2338G>T (CDCA3)	XP_011519331.1:n.*2338G>T
XM_011521030.1:c.*2271G>T (CDCA3)	XP_011519332.1:n.*2271G>T
XM_011520953.3:c.700-177C>A (GNB3)	XP_011519255.1:n.700-177C>A
XR_001748879.2:n.3665G>T (CDCA3)
XR_001748880.2:n.3016G>T (CDCA3)
XR_001748881.2:n.2925G>T (CDCA3)
XR_002957383.1:n.3167G>T (CDCA3)
XR_002957384.1:n.4078G>T (CDCA3)
XR_002957385.1:n.3558G>T (CDCA3)
NM_001297571.2:c.697-177C>A (GNB3)	NP_001284500.1:n.697-177C>A
NM_002075.4:c.700-177C>A (GNB3) MANE Select	NP_002066.1:n.700-177C>A
NM_001297603.3:c.*1379G>T (CDCA3)	NP_001284532.1:n.*1379G>T