Canonical Allele Identifier: CA2014278240

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6845621G= , CM000674.2:g.6845621G= GRCh38
NC_000012.11:g.6954785G= , CM000674.1:g.6954785G= GRCh37
NC_000012.10:g.6825046G= NCBI36
NG_009100.1:g.10411G=
NG_009100.2:g.10411G=

Transcript Alleles

HGVS Amino-acid change
ENST00000229264.8:c.735G= (GNB3) MANE Select ENSP00000229264.3:p.Ser245=
ENST00000229264.7:c.735G= (GNB3) ENSP00000229264.3:p.Ser245=
ENST00000422785.7:c.*1167C= (CDCA3) ENSP00000415142.2:n.*1167C=
ENST00000435982.6:c.732G= (GNB3) ENSP00000414734.2:p.Ser244=
ENST00000537035.1:c.612G= (GNB3) ENSP00000445967.1:p.Ser204=
ENST00000540458.5:n.2086G= (GNB3)
ENST00000542751.1:n.255G= (GNB3)
ENST00000603043.1:n.1233C= (CDCA3)
ENST00000604599.1:n.2095C= (CDCA3)
NM_001297571.1:c.732G= (GNB3) NP_001284500.1:p.Ser244=
NM_002075.3:c.735G= (GNB3) NP_002066.1:p.Ser245=
XM_011520953.1:c.735G= (GNB3) XP_011519255.1:p.Ser245=
XM_011520954.1:c.732G= (GNB3) XP_011519256.1:p.Ser244=
XM_011521027.1:c.*1908C= (CDCA3) XP_011519329.1:n.*1908C=
XM_011521028.1:c.*1908C= (CDCA3) XP_011519330.1:n.*1908C=
XM_011521029.1:c.*2126C= (CDCA3) XP_011519331.1:n.*2126C=
XM_011521030.1:c.*2059C= (CDCA3) XP_011519332.1:n.*2059C=
XM_011520953.3:c.735G= (GNB3) XP_011519255.1:p.Ser245=
XR_001748879.2:n.3453C= (CDCA3)
XR_001748880.2:n.2804C= (CDCA3)
XR_001748881.2:n.2713C= (CDCA3)
XR_002957383.1:n.2955C= (CDCA3)
XR_002957384.1:n.3866C= (CDCA3)
XR_002957385.1:n.3346C= (CDCA3)
NM_001297571.2:c.732G= (GNB3) NP_001284500.1:p.Ser244=
NM_002075.4:c.735G= (GNB3) MANE Select NP_002066.1:p.Ser245=
NM_001297603.3:c.*1167C= (CDCA3) NP_001284532.1:n.*1167C=