Canonical Allele Identifier: CA1216113279
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1675455546
gnomAD v4: 1-193122033-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122033T>C , CM000663.2:g.193122033T>C GRCh38
NC_000001.10:g.193091163T>C , CM000663.1:g.193091163T>C GRCh37
NC_000001.9:g.191357786T>C NCBI36
NG_012691.1:g.5076T>C , LRG_507:g.5076T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-168T>C MANE Select ENSP00000356405.4:n.-168T>C
ENST00000643006.1:c.-168T>C ENSP00000496633.1:n.-168T>C
ENST00000649895.1:n.51T>C
ENST00000367435.3:c.-168T>C ENSP00000356405.3:n.-168T>C
NM_024529.4:c.-168T>C , LRG_507t1:c.-168T>C NP_078805.3:n.-168T>C
XM_006711537.4:c.-168T>C XP_006711600.1:n.-168T>C
XR_001738350.1:n.1624A>G
NM_024529.5:c.-168T>C MANE Select NP_078805.3:n.-168T>C
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