Canonical Allele Identifier: CA729323373
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1291584115
gnomAD v3: 1-193252035-C-G
gnomAD v4: 1-193252035-C-G
MyVariant Identifiers: chr1:g.193221165C>G (hg19) chr1:g.193252035C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193252035C>G , CM000663.2:g.193252035C>G GRCh38
NC_000001.10:g.193221165C>G , CM000663.1:g.193221165C>G GRCh37
NC_000001.9:g.191487788C>G NCBI36
NG_012691.1:g.135078C>G , LRG_507:g.135078C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1323C>G MANE Select ENSP00000356405.4:n.*1323C>G
ENST00000635846.1:c.*1323C>G ENSP00000490035.1:n.*1323C>G
ENST00000643006.1:c.*1829C>G ENSP00000496633.1:n.*1829C>G
ENST00000367435.3:c.*1323C>G ENSP00000356405.3:n.*1323C>G
NM_024529.4:c.*1323C>G , LRG_507t1:c.*1323C>G NP_078805.3:n.*1323C>G
NM_024529.5:c.*1323C>G MANE Select NP_078805.3:n.*1323C>G
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