Canonical Allele Identifier: CA729322963
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1312164646

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251445T>C , CM000663.2:g.193251445T>C GRCh38
NC_000001.10:g.193220575T>C , CM000663.1:g.193220575T>C GRCh37
NC_000001.9:g.191487198T>C NCBI36
NG_012691.1:g.134488T>C , LRG_507:g.134488T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*733T>C MANE Select ENSP00000356405.4:n.*733T>C
ENST00000635846.1:c.*733T>C ENSP00000490035.1:n.*733T>C
ENST00000643006.1:c.*1239T>C ENSP00000496633.1:n.*1239T>C
ENST00000367435.3:c.*733T>C ENSP00000356405.3:n.*733T>C
NM_024529.4:c.*733T>C , LRG_507t1:c.*733T>C NP_078805.3:n.*733T>C
NM_024529.5:c.*733T>C MANE Select NP_078805.3:n.*733T>C