Canonical Allele Identifier: CA2697535999
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs996130368
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122024C>A , CM000663.2:g.193122024C>A GRCh38
NC_000001.10:g.193091154C>A , CM000663.1:g.193091154C>A GRCh37
NC_000001.9:g.191357777C>A NCBI36
NG_012691.1:g.5067C>A , LRG_507:g.5067C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000643006.1:c.-177C>A ENSP00000496633.1:n.-177C>A
ENST00000649895.1:n.42C>A
ENST00000367435.3:c.-177C>A ENSP00000356405.3:n.-177C>A
NM_024529.4:c.-177C>A , LRG_507t1:c.-177C>A NP_078805.3:n.-177C>A
XR_001738350.1:n.1633G>T
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