Canonical Allele Identifier: CA528019095
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1160642140
gnomAD v2: 1-193220607-A-G
gnomAD v4: 1-193251477-A-G
MyVariant Identifiers: chr1:g.193220607A>G (hg19) chr1:g.193251477A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251477A>G , CM000663.2:g.193251477A>G GRCh38
NC_000001.10:g.193220607A>G , CM000663.1:g.193220607A>G GRCh37
NC_000001.9:g.191487230A>G NCBI36
NG_012691.1:g.134520A>G , LRG_507:g.134520A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*765A>G MANE Select ENSP00000356405.4:n.*765A>G
ENST00000635846.1:c.*765A>G ENSP00000490035.1:n.*765A>G
ENST00000643006.1:c.*1271A>G ENSP00000496633.1:n.*1271A>G
ENST00000367435.3:c.*765A>G ENSP00000356405.3:n.*765A>G
NM_024529.4:c.*765A>G , LRG_507t1:c.*765A>G NP_078805.3:n.*765A>G
NM_024529.5:c.*765A>G MANE Select NP_078805.3:n.*765A>G
Search 100 bp 5'
Search 100 bp 3'