Canonical Allele Identifier: CA6417429

Gene: GNB3

Linked Data

• ClinVar Variation Id: 1937606
• ClinVar RCV Id: RCV002653346
• dbSNP Id: rs782501836
• ExAC: 12:6952186 C / T
• gnomAD v2: 12-6952186-C-T
• gnomAD v3: 12-6843022-C-T
• gnomAD v4: 12-6843022-C-T
• COSMIC: COSM431759
• MyVariant Identifiers: chr12:g.6952186C>T (hg19) ; chr12:g.6843022C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6843022C>T , CM000674.2:g.6843022C>T	GRCh38
NC_000012.11:g.6952186C>T , CM000674.1:g.6952186C>T	GRCh37
NC_000012.10:g.6822447C>T	NCBI36
NG_009100.1:g.7812C>T
NG_009100.2:g.7812C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.149C>T MANE Select	ENSP00000229264.3:p.Thr50Met
ENST00000229264.7:c.149C>T	ENSP00000229264.3:p.Thr50Met
ENST00000435982.6:c.149C>T	ENSP00000414734.2:p.Thr50Met
ENST00000537035.1:c.149C>T	ENSP00000445967.1:p.Thr50Met
ENST00000539127.5:c.*169C>T	ENSP00000444325.1:n.*169C>T
ENST00000540458.5:n.1500C>T
ENST00000541257.5:c.149C>T	ENSP00000442002.1:p.Thr50Met
ENST00000541978.5:c.149C>T	ENSP00000439753.2:p.Thr50Met
NM_001297571.1:c.149C>T	NP_001284500.1:p.Thr50Met
NM_002075.3:c.149C>T	NP_002066.1:p.Thr50Met
XM_011520953.1:c.149C>T	XP_011519255.1:p.Thr50Met
XM_011520954.1:c.149C>T	XP_011519256.1:p.Thr50Met
XM_011520953.3:c.149C>T	XP_011519255.1:p.Thr50Met
NM_001297571.2:c.149C>T	NP_001284500.1:p.Thr50Met
NM_002075.4:c.149C>T MANE Select	NP_002066.1:p.Thr50Met