Canonical Allele Identifier: CA35103591
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1001568230
gnomAD v3: 1-193251774-C-T
gnomAD v4: 1-193251774-C-T
MyVariant Identifiers: chr1:g.193220904C>T (hg19) chr1:g.193251774C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251774C>T , CM000663.2:g.193251774C>T GRCh38
NC_000001.10:g.193220904C>T , CM000663.1:g.193220904C>T GRCh37
NC_000001.9:g.191487527C>T NCBI36
NG_012691.1:g.134817C>T , LRG_507:g.134817C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1062C>T MANE Select ENSP00000356405.4:n.*1062C>T
ENST00000635846.1:c.*1062C>T ENSP00000490035.1:n.*1062C>T
ENST00000643006.1:c.*1568C>T ENSP00000496633.1:n.*1568C>T
ENST00000367435.3:c.*1062C>T ENSP00000356405.3:n.*1062C>T
NM_024529.4:c.*1062C>T , LRG_507t1:c.*1062C>T NP_078805.3:n.*1062C>T
NM_024529.5:c.*1062C>T MANE Select NP_078805.3:n.*1062C>T
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