Canonical Allele Identifier: CA3266439
Gene: CDC20B HGNC NCBI

Linked Data

dbSNP Id: rs776336592
ExAC: 5:54466463 C / T
gnomAD v2: 5-54466463-C-T
gnomAD v3: 5-55170635-C-T
gnomAD v4: 5-55170635-C-T
MyVariant Identifiers: chr5:g.54466463C>T (hg19) chr5:g.55170635C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55170635C>T , CM000667.2:g.55170635C>T GRCh38
NC_000005.9:g.54466463C>T , CM000667.1:g.54466463C>T GRCh37
NC_000005.8:g.54502220C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381375.7:c.126+1953G>A MANE Select ENSP00000370781.2:n.126+1953G>A
ENST00000296733.5:c.126+1953G>A ENSP00000296733.1:n.126+1953G>A
ENST00000322374.10:c.126+1953G>A ENSP00000315720.6:n.126+1953G>A
ENST00000381375.6:c.126+1953G>A ENSP00000370781.2:n.126+1953G>A
ENST00000507931.1:c.63+2303G>A ENSP00000423919.1:n.63+2303G>A
ENST00000513180.5:c.126+1953G>A ENSP00000426776.1:n.126+1953G>A
NM_001145734.2:c.126+1953G>A NP_001139206.2:n.126+1953G>A
NM_001170402.1:c.126+1953G>A MANE Select NP_001163873.1:n.126+1953G>A
NM_152623.2:c.126+1953G>A NP_689836.2:n.126+1953G>A
XM_011543218.1:c.126+1953G>A XP_011541520.1:n.126+1953G>A
XM_011543218.2:c.126+1953G>A XP_011541520.1:n.126+1953G>A
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