Canonical Allele Identifier: CA527707657
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1259484490
gnomAD v2: 1-193091095-C-A
gnomAD v4: 1-193121965-C-A
MyVariant Identifiers: chr1:g.193091095C>A (hg19) chr1:g.193121965C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121965C>A , CM000663.2:g.193121965C>A GRCh38
NC_000001.10:g.193091095C>A , CM000663.1:g.193091095C>A GRCh37
NC_000001.9:g.191357718C>A NCBI36
NG_012691.1:g.5008C>A , LRG_507:g.5008C>A

Transcript Alleles

HGVS Amino-acid Change
NM_024529.4:c.-236C>A , LRG_507t1:c.-236C>A NP_078805.3:n.-236C>A
XR_001738350.1:n.1692G>T
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