Canonical Allele Identifier: CA2697810911
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103111112

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122019G>A , CM000663.2:g.193122019G>A GRCh38
NC_000001.10:g.193091149G>A , CM000663.1:g.193091149G>A GRCh37
NC_000001.9:g.191357772G>A NCBI36
NG_012691.1:g.5062G>A , LRG_507:g.5062G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000643006.1:c.-182G>A ENSP00000496633.1:n.-182G>A
ENST00000649895.1:n.37G>A
ENST00000367435.3:c.-182G>A ENSP00000356405.3:n.-182G>A
NM_024529.4:c.-182G>A , LRG_507t1:c.-182G>A NP_078805.3:n.-182G>A
XR_001738350.1:n.1638C>T