Canonical Allele Identifier: CA383671561
Gene: GNB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6842979G>C , CM000674.2:g.6842979G>C GRCh38
NC_000012.11:g.6952143G>C , CM000674.1:g.6952143G>C GRCh37
NC_000012.10:g.6822404G>C NCBI36
NG_009100.1:g.7769G>C
NG_009100.2:g.7769G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000229264.8:c.106G>C MANE Select ENSP00000229264.3:p.Gly36Arg
ENST00000229264.7:c.106G>C ENSP00000229264.3:p.Gly36Arg
ENST00000435982.6:c.106G>C ENSP00000414734.2:p.Gly36Arg
ENST00000537035.1:c.106G>C ENSP00000445967.1:p.Gly36Arg
ENST00000539127.5:c.*126G>C ENSP00000444325.1:n.*126G>C
ENST00000540458.5:n.1457G>C
ENST00000541257.5:c.106G>C ENSP00000442002.1:p.Gly36Arg
ENST00000541978.5:c.106G>C ENSP00000439753.2:p.Gly36Arg
ENST00000542868.1:n.594G>C
NM_001297571.1:c.106G>C NP_001284500.1:p.Gly36Arg
NM_002075.3:c.106G>C NP_002066.1:p.Gly36Arg
XM_011520953.1:c.106G>C XP_011519255.1:p.Gly36Arg
XM_011520954.1:c.106G>C XP_011519256.1:p.Gly36Arg
XM_011520953.3:c.106G>C XP_011519255.1:p.Gly36Arg
NM_001297571.2:c.106G>C NP_001284500.1:p.Gly36Arg
NM_002075.4:c.106G>C MANE Select NP_002066.1:p.Gly36Arg