Canonical Allele Identifier: CA2697810937
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103111123

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122023C>G , CM000663.2:g.193122023C>G GRCh38
NC_000001.10:g.193091153C>G , CM000663.1:g.193091153C>G GRCh37
NC_000001.9:g.191357776C>G NCBI36
NG_012691.1:g.5066C>G , LRG_507:g.5066C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000643006.1:c.-178C>G ENSP00000496633.1:n.-178C>G
ENST00000649895.1:n.41C>G
ENST00000367435.3:c.-178C>G ENSP00000356405.3:n.-178C>G
NM_024529.4:c.-178C>G , LRG_507t1:c.-178C>G NP_078805.3:n.-178C>G
XR_001738350.1:n.1634G>C