Canonical Allele Identifier: CA2014278192

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6845536G= , CM000674.2:g.6845536G= GRCh38
NC_000012.11:g.6954700G= , CM000674.1:g.6954700G= GRCh37
NC_000012.10:g.6824961G= NCBI36
NG_009100.1:g.10326G=
NG_009100.2:g.10326G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229264.8:c.700-50G= (GNB3) MANE Select ENSP00000229264.3:n.700-50G=
ENST00000229264.7:c.700-50G= (GNB3) ENSP00000229264.3:n.700-50G=
ENST00000422785.7:c.*1252C= (CDCA3) ENSP00000415142.2:n.*1252C=
ENST00000435982.6:c.697-50G= (GNB3) ENSP00000414734.2:n.697-50G=
ENST00000537035.1:c.577-50G= (GNB3) ENSP00000445967.1:n.577-50G=
ENST00000540458.5:n.2051-50G= (GNB3)
ENST00000542751.1:n.170G= (GNB3)
ENST00000603043.1:n.1318C= (CDCA3)
ENST00000604599.1:n.2180C= (CDCA3)
NM_001297571.1:c.697-50G= (GNB3) NP_001284500.1:n.697-50G=
NM_002075.3:c.700-50G= (GNB3) NP_002066.1:n.700-50G=
XM_011520953.1:c.700-50G= (GNB3) XP_011519255.1:n.700-50G=
XM_011520954.1:c.697-50G= (GNB3) XP_011519256.1:n.697-50G=
XM_011521027.1:c.*1993C= (CDCA3) XP_011519329.1:n.*1993C=
XM_011521028.1:c.*1993C= (CDCA3) XP_011519330.1:n.*1993C=
XM_011521029.1:c.*2211C= (CDCA3) XP_011519331.1:n.*2211C=
XM_011521030.1:c.*2144C= (CDCA3) XP_011519332.1:n.*2144C=
XM_011520953.3:c.700-50G= (GNB3) XP_011519255.1:n.700-50G=
XR_001748879.2:n.3538C= (CDCA3)
XR_001748880.2:n.2889C= (CDCA3)
XR_001748881.2:n.2798C= (CDCA3)
XR_002957383.1:n.3040C= (CDCA3)
XR_002957384.1:n.3951C= (CDCA3)
XR_002957385.1:n.3431C= (CDCA3)
NM_001297571.2:c.697-50G= (GNB3) NP_001284500.1:n.697-50G=
NM_002075.4:c.700-50G= (GNB3) MANE Select NP_002066.1:n.700-50G=
NM_001297603.3:c.*1252C= (CDCA3) NP_001284532.1:n.*1252C=