Canonical Allele Identifier: CA1216171022
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1678041772

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251458C>G , CM000663.2:g.193251458C>G GRCh38
NC_000001.10:g.193220588C>G , CM000663.1:g.193220588C>G GRCh37
NC_000001.9:g.191487211C>G NCBI36
NG_012691.1:g.134501C>G , LRG_507:g.134501C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*746C>G MANE Select ENSP00000356405.4:n.*746C>G
ENST00000635846.1:c.*746C>G ENSP00000490035.1:n.*746C>G
ENST00000643006.1:c.*1252C>G ENSP00000496633.1:n.*1252C>G
ENST00000367435.3:c.*746C>G ENSP00000356405.3:n.*746C>G
NM_024529.4:c.*746C>G , LRG_507t1:c.*746C>G NP_078805.3:n.*746C>G
NM_024529.5:c.*746C>G MANE Select NP_078805.3:n.*746C>G