Canonical Allele Identifier: CA2697810862
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103111107
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122013T>A , CM000663.2:g.193122013T>A GRCh38
NC_000001.10:g.193091143T>A , CM000663.1:g.193091143T>A GRCh37
NC_000001.9:g.191357766T>A NCBI36
NG_012691.1:g.5056T>A , LRG_507:g.5056T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000643006.1:c.-188T>A ENSP00000496633.1:n.-188T>A
ENST00000649895.1:n.31T>A
NM_024529.4:c.-188T>A , LRG_507t1:c.-188T>A NP_078805.3:n.-188T>A
XR_001738350.1:n.1644A>T
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