Canonical Allele Identifier: CA1010619085
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1678049618
gnomAD v3: 1-193251893-T-G
gnomAD v4: 1-193251893-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251893T>G , CM000663.2:g.193251893T>G GRCh38
NC_000001.10:g.193221023T>G , CM000663.1:g.193221023T>G GRCh37
NC_000001.9:g.191487646T>G NCBI36
NG_012691.1:g.134936T>G , LRG_507:g.134936T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1181T>G MANE Select ENSP00000356405.4:n.*1181T>G
ENST00000635846.1:c.*1181T>G ENSP00000490035.1:n.*1181T>G
ENST00000643006.1:c.*1687T>G ENSP00000496633.1:n.*1687T>G
ENST00000367435.3:c.*1181T>G ENSP00000356405.3:n.*1181T>G
NM_024529.4:c.*1181T>G , LRG_507t1:c.*1181T>G NP_078805.3:n.*1181T>G
NM_024529.5:c.*1181T>G MANE Select NP_078805.3:n.*1181T>G
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