Canonical Allele Identifier: CA729323094
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1196005073
MyVariant Identifiers: chr1:g.193220828A>G (hg19) chr1:g.193251698A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251698A>G , CM000663.2:g.193251698A>G GRCh38
NC_000001.10:g.193220828A>G , CM000663.1:g.193220828A>G GRCh37
NC_000001.9:g.191487451A>G NCBI36
NG_012691.1:g.134741A>G , LRG_507:g.134741A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*986A>G MANE Select ENSP00000356405.4:n.*986A>G
ENST00000635846.1:c.*986A>G ENSP00000490035.1:n.*986A>G
ENST00000643006.1:c.*1492A>G ENSP00000496633.1:n.*1492A>G
ENST00000367435.3:c.*986A>G ENSP00000356405.3:n.*986A>G
NM_024529.4:c.*986A>G , LRG_507t1:c.*986A>G NP_078805.3:n.*986A>G
NM_024529.5:c.*986A>G MANE Select NP_078805.3:n.*986A>G
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