Canonical Allele Identifier: CA1010608077
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1489931121
gnomAD v3: 1-193122009-G-C
gnomAD v4: 1-193122009-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122009G>C , CM000663.2:g.193122009G>C GRCh38
NC_000001.10:g.193091139G>C , CM000663.1:g.193091139G>C GRCh37
NC_000001.9:g.191357762G>C NCBI36
NG_012691.1:g.5052G>C , LRG_507:g.5052G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000643006.1:c.-192G>C ENSP00000496633.1:n.-192G>C
ENST00000649895.1:n.27G>C
NM_024529.4:c.-192G>C , LRG_507t1:c.-192G>C NP_078805.3:n.-192G>C
XR_001738350.1:n.1648C>G
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