Canonical Allele Identifier: CA2649631048
Gene: CDC73 HGNC NCBI

Linked Data

gnomAD v4: 1-193251567-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251567G>C , CM000663.2:g.193251567G>C GRCh38
NC_000001.10:g.193220697G>C , CM000663.1:g.193220697G>C GRCh37
NC_000001.9:g.191487320G>C NCBI36
NG_012691.1:g.134610G>C , LRG_507:g.134610G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*855G>C MANE Select ENSP00000356405.4:n.*855G>C
ENST00000635846.1:c.*855G>C ENSP00000490035.1:n.*855G>C
ENST00000643006.1:c.*1361G>C ENSP00000496633.1:n.*1361G>C
ENST00000367435.3:c.*855G>C ENSP00000356405.3:n.*855G>C
NM_024529.4:c.*855G>C , LRG_507t1:c.*855G>C NP_078805.3:n.*855G>C
NM_024529.5:c.*855G>C MANE Select NP_078805.3:n.*855G>C
Search 100 bp 5'
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