Canonical Allele Identifier: CA383671689

Gene: GNB3

Linked Data

• gnomAD v4: 12-6843024-T-G
• MyVariant Identifiers: chr12:g.6952188T>G (hg19) ; chr12:g.6843024T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6843024T>G , CM000674.2:g.6843024T>G	GRCh38
NC_000012.11:g.6952188T>G , CM000674.1:g.6952188T>G	GRCh37
NC_000012.10:g.6822449T>G	NCBI36
NG_009100.1:g.7814T>G
NG_009100.2:g.7814T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229264.8:c.151T>G MANE Select	ENSP00000229264.3:p.Leu51Val
ENST00000229264.7:c.151T>G	ENSP00000229264.3:p.Leu51Val
ENST00000435982.6:c.151T>G	ENSP00000414734.2:p.Leu51Val
ENST00000537035.1:c.151T>G	ENSP00000445967.1:p.Leu51Val
ENST00000539127.5:c.*171T>G	ENSP00000444325.1:n.*171T>G
ENST00000540458.5:n.1502T>G
ENST00000541257.5:c.151T>G	ENSP00000442002.1:p.Leu51Val
ENST00000541978.5:c.151T>G	ENSP00000439753.2:p.Leu51Val
NM_001297571.1:c.151T>G	NP_001284500.1:p.Leu51Val
NM_002075.3:c.151T>G	NP_002066.1:p.Leu51Val
XM_011520953.1:c.151T>G	XP_011519255.1:p.Leu51Val
XM_011520954.1:c.151T>G	XP_011519256.1:p.Leu51Val
XM_011520953.3:c.151T>G	XP_011519255.1:p.Leu51Val
NM_001297571.2:c.151T>G	NP_001284500.1:p.Leu51Val
NM_002075.4:c.151T>G MANE Select	NP_002066.1:p.Leu51Val