Canonical Allele Identifier: CA383671651
Gene: GNB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6843007T>G , CM000674.2:g.6843007T>G GRCh38
NC_000012.11:g.6952171T>G , CM000674.1:g.6952171T>G GRCh37
NC_000012.10:g.6822432T>G NCBI36
NG_009100.1:g.7797T>G
NG_009100.2:g.7797T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000229264.8:c.134T>G MANE Select ENSP00000229264.3:p.Met45Arg
ENST00000229264.7:c.134T>G ENSP00000229264.3:p.Met45Arg
ENST00000435982.6:c.134T>G ENSP00000414734.2:p.Met45Arg
ENST00000537035.1:c.134T>G ENSP00000445967.1:p.Met45Arg
ENST00000539127.5:c.*154T>G ENSP00000444325.1:n.*154T>G
ENST00000540458.5:n.1485T>G
ENST00000541257.5:c.134T>G ENSP00000442002.1:p.Met45Arg
ENST00000541978.5:c.134T>G ENSP00000439753.2:p.Met45Arg
NM_001297571.1:c.134T>G NP_001284500.1:p.Met45Arg
NM_002075.3:c.134T>G NP_002066.1:p.Met45Arg
XM_011520953.1:c.134T>G XP_011519255.1:p.Met45Arg
XM_011520954.1:c.134T>G XP_011519256.1:p.Met45Arg
XM_011520953.3:c.134T>G XP_011519255.1:p.Met45Arg
NM_001297571.2:c.134T>G NP_001284500.1:p.Met45Arg
NM_002075.4:c.134T>G MANE Select NP_002066.1:p.Met45Arg