Canonical Allele Identifier: CA383675202

Gene: GNB3 CDCA3

Linked Data

• MyVariant Identifiers: chr12:g.6954885T>C (hg19) ; chr12:g.6845721T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6845721T>C , CM000674.2:g.6845721T>C	GRCh38
NC_000012.11:g.6954885T>C , CM000674.1:g.6954885T>C	GRCh37
NC_000012.10:g.6825146T>C	NCBI36
NG_009100.1:g.10511T>C
NG_009100.2:g.10511T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000229264.8:c.835T>C (GNB3) MANE Select	ENSP00000229264.3:p.Ser279Pro
ENST00000229264.7:c.835T>C (GNB3)	ENSP00000229264.3:p.Ser279Pro
ENST00000422785.7:c.*1067A>G (CDCA3)	ENSP00000415142.2:n.*1067A>G
ENST00000435982.6:c.832T>C (GNB3)	ENSP00000414734.2:p.Ser278Pro
ENST00000537035.1:c.712T>C (GNB3)	ENSP00000445967.1:p.Ser238Pro
ENST00000540458.5:n.2186T>C (GNB3)
ENST00000542751.1:n.355T>C (GNB3)
ENST00000603043.1:n.1133A>G (CDCA3)
ENST00000604599.1:n.1995A>G (CDCA3)
NM_001297571.1:c.832T>C (GNB3)	NP_001284500.1:p.Ser278Pro
NM_002075.3:c.835T>C (GNB3)	NP_002066.1:p.Ser279Pro
XM_011520953.1:c.835T>C (GNB3)	XP_011519255.1:p.Ser279Pro
XM_011520954.1:c.832T>C (GNB3)	XP_011519256.1:p.Ser278Pro
XM_011521027.1:c.*1808A>G (CDCA3)	XP_011519329.1:n.*1808A>G
XM_011521028.1:c.*1808A>G (CDCA3)	XP_011519330.1:n.*1808A>G
XM_011521029.1:c.*2026A>G (CDCA3)	XP_011519331.1:n.*2026A>G
XM_011521030.1:c.*1959A>G (CDCA3)	XP_011519332.1:n.*1959A>G
XM_011520953.3:c.835T>C (GNB3)	XP_011519255.1:p.Ser279Pro
XR_001748879.2:n.3353A>G (CDCA3)
XR_001748880.2:n.2704A>G (CDCA3)
XR_001748881.2:n.2613A>G (CDCA3)
XR_002957383.1:n.2855A>G (CDCA3)
XR_002957384.1:n.3766A>G (CDCA3)
XR_002957385.1:n.3246A>G (CDCA3)
NM_001297571.2:c.832T>C (GNB3)	NP_001284500.1:p.Ser278Pro
NM_002075.4:c.835T>C (GNB3) MANE Select	NP_002066.1:p.Ser279Pro
NM_001297603.3:c.*1067A>G (CDCA3)	NP_001284532.1:n.*1067A>G