Canonical Allele Identifier: CA34407550

Gene: CDC73

Linked Data

• dbSNP Id: rs949584576
• gnomAD v3: 1-193121989-G-A
• gnomAD v4: 1-193121989-G-A
• MyVariant Identifiers: chr1:g.193091119G>A (hg19) ; chr1:g.193121989G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193121989G>A , CM000663.2:g.193121989G>A	GRCh38
NC_000001.10:g.193091119G>A , CM000663.1:g.193091119G>A	GRCh37
NC_000001.9:g.191357742G>A	NCBI36
NG_012691.1:g.5032G>A , LRG_507:g.5032G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649895.1:n.7G>A
NM_024529.4:c.-212G>A , LRG_507t1:c.-212G>A	NP_078805.3:n.-212G>A
XR_001738350.1:n.1668C>T