Canonical Allele Identifier: CA10609155
Gene: CDC73 HGNC NCBI

Linked Data

ClinVar Variation Id: 294432
ClinVar RCV Id: RCV000260300 RCV000304477 RCV000361563 RCV001797075
dbSNP Id: rs78218016
gnomAD v2: 1-193221109-A-G
gnomAD v3: 1-193251979-A-G
gnomAD v4: 1-193251979-A-G
MyVariant Identifiers: chr1:g.193221109A>G (hg19) chr1:g.193251979A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251979A>G , CM000663.2:g.193251979A>G GRCh38
NC_000001.10:g.193221109A>G , CM000663.1:g.193221109A>G GRCh37
NC_000001.9:g.191487732A>G NCBI36
NG_012691.1:g.135022A>G , LRG_507:g.135022A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1267A>G MANE Select ENSP00000356405.4:n.*1267A>G
ENST00000635846.1:c.*1267A>G ENSP00000490035.1:n.*1267A>G
ENST00000643006.1:c.*1773A>G ENSP00000496633.1:n.*1773A>G
ENST00000367435.3:c.*1267A>G ENSP00000356405.3:n.*1267A>G
NM_024529.4:c.*1267A>G , LRG_507t1:c.*1267A>G NP_078805.3:n.*1267A>G
NM_024529.5:c.*1267A>G MANE Select NP_078805.3:n.*1267A>G
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