Canonical Allele Identifier: CA2794430286
Gene: GNB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6843091_6843092dup , CM000674.2:g.6843091_6843092dup GRCh38
NC_000012.11:g.6952255_6952256dup , CM000674.1:g.6952255_6952256dup GRCh37
NC_000012.10:g.6822516_6822517dup NCBI36
NG_009100.1:g.7881_7882dup
NG_009100.2:g.7881_7882dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000229264.8:c.203+15_203+16dup MANE Select ENSP00000229264.3:n.203+15_203+16dup
ENST00000229264.7:c.203+15_203+16dup ENSP00000229264.3:n.203+15_203+16dup
ENST00000435982.6:c.203+15_203+16dup ENSP00000414734.2:n.203+15_203+16dup
ENST00000537035.1:c.203+15_203+16dup ENSP00000445967.1:n.203+15_203+16dup
ENST00000539127.5:c.*223+15_*223+16dup ENSP00000444325.1:n.*223+15_*223+16dup
ENST00000540458.5:n.1554+15_1554+16dup
ENST00000541257.5:c.203+15_203+16dup ENSP00000442002.1:n.203+15_203+16dup
ENST00000541978.5:c.203+15_203+16dup ENSP00000439753.2:n.203+15_203+16dup
NM_001297571.1:c.203+15_203+16dup NP_001284500.1:n.203+15_203+16dup
NM_002075.3:c.203+15_203+16dup NP_002066.1:n.203+15_203+16dup
XM_011520953.1:c.203+15_203+16dup XP_011519255.1:n.203+15_203+16dup
XM_011520954.1:c.203+15_203+16dup XP_011519256.1:n.203+15_203+16dup
XM_011520953.3:c.203+15_203+16dup XP_011519255.1:n.203+15_203+16dup
NM_001297571.2:c.203+15_203+16dup NP_001284500.1:n.203+15_203+16dup
NM_002075.4:c.203+15_203+16dup MANE Select NP_002066.1:n.203+15_203+16dup