Linked Data
dbSNP Id:
rs10061133
ExAC:
5:54466544 A / G
gnomAD v2:
5-54466544-A-G
gnomAD v3:
5-55170716-A-G
gnomAD v4:
5-55170716-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55170716A>G , CM000667.2:g.55170716A>G | GRCh38 |
| NC_000005.9:g.54466544A>G , CM000667.1:g.54466544A>G | GRCh37 |
| NC_000005.8:g.54502301A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000381375.7:c.126+1872T>C (CDC20B) MANE Select | ENSP00000370781.2:n.126+1872T>C | |
| ENST00000296733.5:c.126+1872T>C (CDC20B) | ENSP00000296733.1:n.126+1872T>C | |
| ENST00000322374.10:c.126+1872T>C (CDC20B) | ENSP00000315720.6:n.126+1872T>C | |
| ENST00000381375.6:c.126+1872T>C (CDC20B) | ENSP00000370781.2:n.126+1872T>C | |
| ENST00000507931.1:c.63+2222T>C (CDC20B) | ENSP00000423919.1:n.63+2222T>C | |
| ENST00000513180.5:c.126+1872T>C (CDC20B) | ENSP00000426776.1:n.126+1872T>C | |
| NM_001145734.2:c.126+1872T>C (CDC20B) | NP_001139206.2:n.126+1872T>C | |
| NM_001170402.1:c.126+1872T>C (CDC20B) MANE Select | NP_001163873.1:n.126+1872T>C | |
| NM_152623.2:c.126+1872T>C (CDC20B) | NP_689836.2:n.126+1872T>C | |
| NR_030387.1:n.27T>C (MIR449B) | ||
| XM_011543218.1:c.126+1872T>C (CDC20B) | XP_011541520.1:n.126+1872T>C | |
| XM_011543218.2:c.126+1872T>C (CDC20B) | XP_011541520.1:n.126+1872T>C |