Canonical Allele Identifier: CA729343908

Gene: CDC73

Linked Data

• dbSNP Id: rs1443039900
• gnomAD v3: 1-193121982-C-T
• gnomAD v4: 1-193121982-C-T
• MyVariant Identifiers: chr1:g.193091112C>T (hg19) ; chr1:g.193121982C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193121982C>T , CM000663.2:g.193121982C>T	GRCh38
NC_000001.10:g.193091112C>T , CM000663.1:g.193091112C>T	GRCh37
NC_000001.9:g.191357735C>T	NCBI36
NG_012691.1:g.5025C>T , LRG_507:g.5025C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.4:c.-219C>T , LRG_507t1:c.-219C>T	NP_078805.3:n.-219C>T
XR_001738350.1:n.1675G>A