Canonical Allele Identifier: CA2649631128
Gene: CDC73 HGNC NCBI

Linked Data

gnomAD v4: 1-193252008-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193252008C>T , CM000663.2:g.193252008C>T GRCh38
NC_000001.10:g.193221138C>T , CM000663.1:g.193221138C>T GRCh37
NC_000001.9:g.191487761C>T NCBI36
NG_012691.1:g.135051C>T , LRG_507:g.135051C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1296C>T MANE Select ENSP00000356405.4:n.*1296C>T
ENST00000635846.1:c.*1296C>T ENSP00000490035.1:n.*1296C>T
ENST00000643006.1:c.*1802C>T ENSP00000496633.1:n.*1802C>T
ENST00000367435.3:c.*1296C>T ENSP00000356405.3:n.*1296C>T
NM_024529.4:c.*1296C>T , LRG_507t1:c.*1296C>T NP_078805.3:n.*1296C>T
NM_024529.5:c.*1296C>T MANE Select NP_078805.3:n.*1296C>T
Search 100 bp 5'
Search 100 bp 3'