Canonical Allele Identifier: CA2649631032
Gene: CDC73 HGNC NCBI

Linked Data

gnomAD v4: 1-193251506-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251506A>G , CM000663.2:g.193251506A>G GRCh38
NC_000001.10:g.193220636A>G , CM000663.1:g.193220636A>G GRCh37
NC_000001.9:g.191487259A>G NCBI36
NG_012691.1:g.134549A>G , LRG_507:g.134549A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*794A>G MANE Select ENSP00000356405.4:n.*794A>G
ENST00000635846.1:c.*794A>G ENSP00000490035.1:n.*794A>G
ENST00000643006.1:c.*1300A>G ENSP00000496633.1:n.*1300A>G
ENST00000367435.3:c.*794A>G ENSP00000356405.3:n.*794A>G
NM_024529.4:c.*794A>G , LRG_507t1:c.*794A>G NP_078805.3:n.*794A>G
NM_024529.5:c.*794A>G MANE Select NP_078805.3:n.*794A>G
Search 100 bp 5'
Search 100 bp 3'