Canonical Allele Identifier: CA2606575216
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs367704451
gnomAD v3: 1-193251795-A-G
gnomAD v4: 1-193251795-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251795A>G , CM000663.2:g.193251795A>G GRCh38
NC_000001.10:g.193220925A>G , CM000663.1:g.193220925A>G GRCh37
NC_000001.9:g.191487548A>G NCBI36
NG_012691.1:g.134838A>G , LRG_507:g.134838A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1083A>G MANE Select ENSP00000356405.4:n.*1083A>G
ENST00000635846.1:c.*1083A>G ENSP00000490035.1:n.*1083A>G
ENST00000643006.1:c.*1589A>G ENSP00000496633.1:n.*1589A>G
ENST00000367435.3:c.*1083A>G ENSP00000356405.3:n.*1083A>G
NM_024529.4:c.*1083A>G , LRG_507t1:c.*1083A>G NP_078805.3:n.*1083A>G
NM_024529.5:c.*1083A>G MANE Select NP_078805.3:n.*1083A>G
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