Canonical Allele Identifier: CA6417466
Gene: GNB3 HGNC NCBI

Linked Data

dbSNP Id: rs782044718
gnomAD v2: 12-6952305-A-T
gnomAD v4: 12-6843141-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6843141A>T , CM000674.2:g.6843141A>T GRCh38
NC_000012.11:g.6952305A>T , CM000674.1:g.6952305A>T GRCh37
NC_000012.10:g.6822566A>T NCBI36
NG_009100.1:g.7931A>T
NG_009100.2:g.7931A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229264.8:c.204-33A>T MANE Select ENSP00000229264.3:n.204-33A>T
ENST00000229264.7:c.204-33A>T ENSP00000229264.3:n.204-33A>T
ENST00000435982.6:c.204-33A>T ENSP00000414734.2:n.204-33A>T
ENST00000537035.1:c.204-33A>T ENSP00000445967.1:n.204-33A>T
ENST00000539127.5:c.*224-33A>T ENSP00000444325.1:n.*224-33A>T
ENST00000540458.5:n.1555-33A>T
ENST00000541257.5:c.204-33A>T ENSP00000442002.1:n.204-33A>T
ENST00000541978.5:c.204-33A>T ENSP00000439753.2:n.204-33A>T
NM_001297571.1:c.204-33A>T NP_001284500.1:n.204-33A>T
NM_002075.3:c.204-33A>T NP_002066.1:n.204-33A>T
XM_011520953.1:c.204-33A>T XP_011519255.1:n.204-33A>T
XM_011520954.1:c.204-33A>T XP_011519256.1:n.204-33A>T
XM_011520953.3:c.204-33A>T XP_011519255.1:n.204-33A>T
NM_001297571.2:c.204-33A>T NP_001284500.1:n.204-33A>T
NM_002075.4:c.204-33A>T MANE Select NP_002066.1:n.204-33A>T