Canonical Allele Identifier: CA528019108
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1164598850
gnomAD v2: 1-193220894-T-A
gnomAD v3: 1-193251764-T-A
gnomAD v4: 1-193251764-T-A
MyVariant Identifiers: chr1:g.193220894T>A (hg19) chr1:g.193251764T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251764T>A , CM000663.2:g.193251764T>A GRCh38
NC_000001.10:g.193220894T>A , CM000663.1:g.193220894T>A GRCh37
NC_000001.9:g.191487517T>A NCBI36
NG_012691.1:g.134807T>A , LRG_507:g.134807T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1052T>A MANE Select ENSP00000356405.4:n.*1052T>A
ENST00000635846.1:c.*1052T>A ENSP00000490035.1:n.*1052T>A
ENST00000643006.1:c.*1558T>A ENSP00000496633.1:n.*1558T>A
ENST00000367435.3:c.*1052T>A ENSP00000356405.3:n.*1052T>A
NM_024529.4:c.*1052T>A , LRG_507t1:c.*1052T>A NP_078805.3:n.*1052T>A
NM_024529.5:c.*1052T>A MANE Select NP_078805.3:n.*1052T>A
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