Canonical Allele Identifier: CA2014277008
Gene: GNB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6843073C= , CM000674.2:g.6843073C= GRCh38
NC_000012.11:g.6952237C= , CM000674.1:g.6952237C= GRCh37
NC_000012.10:g.6822498C= NCBI36
NG_009100.1:g.7863C=
NG_009100.2:g.7863C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229264.8:c.200C= MANE Select ENSP00000229264.3:p.Ser67=
ENST00000229264.7:c.200C= ENSP00000229264.3:p.Ser67=
ENST00000435982.6:c.200C= ENSP00000414734.2:p.Ser67=
ENST00000537035.1:c.200C= ENSP00000445967.1:p.Ser67=
ENST00000539127.5:c.*220C= ENSP00000444325.1:n.*220C=
ENST00000540458.5:n.1551C=
ENST00000541257.5:c.200C= ENSP00000442002.1:p.Ser67=
ENST00000541978.5:c.200C= ENSP00000439753.2:p.Ser67=
NM_001297571.1:c.200C= NP_001284500.1:p.Ser67=
NM_002075.3:c.200C= NP_002066.1:p.Ser67=
XM_011520953.1:c.200C= XP_011519255.1:p.Ser67=
XM_011520954.1:c.200C= XP_011519256.1:p.Ser67=
XM_011520953.3:c.200C= XP_011519255.1:p.Ser67=
NM_001297571.2:c.200C= NP_001284500.1:p.Ser67=
NM_002075.4:c.200C= MANE Select NP_002066.1:p.Ser67=