Canonical Allele Identifier: CA2697561614
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1292438529

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121992G>A , CM000663.2:g.193121992G>A GRCh38
NC_000001.10:g.193091122G>A , CM000663.1:g.193091122G>A GRCh37
NC_000001.9:g.191357745G>A NCBI36
NG_012691.1:g.5035G>A , LRG_507:g.5035G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649895.1:n.10G>A
NM_024529.4:c.-209G>A , LRG_507t1:c.-209G>A NP_078805.3:n.-209G>A
XR_001738350.1:n.1665C>T