Canonical Allele Identifier: CA2617344131

Linked Data

gnomAD v4: 12-6847187-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6847187G>T , CM000674.2:g.6847187G>T GRCh38
NC_000012.11:g.6956351G>T , CM000674.1:g.6956351G>T GRCh37
NC_000012.10:g.6826612G>T NCBI36
NG_009100.1:g.11977G>T
NG_009100.2:g.11977G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229264.8:c.*289G>T (GNB3) MANE Select ENSP00000229264.3:n.*289G>T
ENST00000229264.7:c.*289G>T (GNB3) ENSP00000229264.3:n.*289G>T
ENST00000422785.7:c.545-284C>A (CDCA3) ENSP00000415142.2:n.545-284C>A
ENST00000540458.5:n.2663G>T (GNB3)
ENST00000542751.1:n.832G>T (GNB3)
ENST00000603043.1:n.308-284C>A (CDCA3)
ENST00000604599.1:n.813-284C>A (CDCA3)
NM_001297571.1:c.*289G>T (GNB3) NP_001284500.1:n.*289G>T
NM_001297603.1:c.545-284C>A (CDCA3) NP_001284532.1:n.545-284C>A
NM_002075.3:c.*289G>T (GNB3) NP_002066.1:n.*289G>T
XM_011521027.1:c.*983-284C>A (CDCA3) XP_011519329.1:n.*983-284C>A
XM_011521028.1:c.*983-284C>A (CDCA3) XP_011519330.1:n.*983-284C>A
XM_011521029.1:c.*1201-284C>A (CDCA3) XP_011519331.1:n.*1201-284C>A
XM_011521030.1:c.*1134-284C>A (CDCA3) XP_011519332.1:n.*1134-284C>A
NM_001297603.2:c.545-284C>A (CDCA3) NP_001284532.1:n.545-284C>A
XR_001748879.2:n.2528-284C>A (CDCA3)
XR_001748880.2:n.1879-284C>A (CDCA3)
XR_001748881.2:n.1788-284C>A (CDCA3)
XR_002957383.1:n.2030-284C>A (CDCA3)
XR_002957384.1:n.2941-284C>A (CDCA3)
XR_002957385.1:n.2421-284C>A (CDCA3)
NM_001297571.2:c.*289G>T (GNB3) NP_001284500.1:n.*289G>T
NM_002075.4:c.*289G>T (GNB3) MANE Select NP_002066.1:n.*289G>T
NM_001297603.3:c.545-284C>A (CDCA3) NP_001284532.1:n.545-284C>A