Canonical Allele Identifier: CA729322974

Gene: CDC73

Linked Data

• dbSNP Id: rs1375573968
• MyVariant Identifiers: chr1:g.193220594A>G (hg19) ; chr1:g.193251464A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193251464A>G , CM000663.2:g.193251464A>G	GRCh38
NC_000001.10:g.193220594A>G , CM000663.1:g.193220594A>G	GRCh37
NC_000001.9:g.191487217A>G	NCBI36
NG_012691.1:g.134507A>G , LRG_507:g.134507A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.*752A>G MANE Select	ENSP00000356405.4:n.*752A>G
ENST00000635846.1:c.*752A>G	ENSP00000490035.1:n.*752A>G
ENST00000643006.1:c.*1258A>G	ENSP00000496633.1:n.*1258A>G
ENST00000367435.3:c.*752A>G	ENSP00000356405.3:n.*752A>G
NM_024529.4:c.*752A>G , LRG_507t1:c.*752A>G	NP_078805.3:n.*752A>G
NM_024529.5:c.*752A>G MANE Select	NP_078805.3:n.*752A>G