Canonical Allele Identifier: CA2649631121
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2102075767
gnomAD v4: 1-193251958-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251958C>T , CM000663.2:g.193251958C>T GRCh38
NC_000001.10:g.193221088C>T , CM000663.1:g.193221088C>T GRCh37
NC_000001.9:g.191487711C>T NCBI36
NG_012691.1:g.135001C>T , LRG_507:g.135001C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1246C>T MANE Select ENSP00000356405.4:n.*1246C>T
ENST00000635846.1:c.*1246C>T ENSP00000490035.1:n.*1246C>T
ENST00000643006.1:c.*1752C>T ENSP00000496633.1:n.*1752C>T
ENST00000367435.3:c.*1246C>T ENSP00000356405.3:n.*1246C>T
NM_024529.4:c.*1246C>T , LRG_507t1:c.*1246C>T NP_078805.3:n.*1246C>T
NM_024529.5:c.*1246C>T MANE Select NP_078805.3:n.*1246C>T
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