Canonical Allele Identifier: CA729343945

Gene: CDC73

Linked Data

• dbSNP Id: rs1351734458
• gnomAD v3: 1-193122029-T-G
• gnomAD v4: 1-193122029-T-G
• MyVariant Identifiers: chr1:g.193091159T>G (hg19) ; chr1:g.193122029T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122029T>G , CM000663.2:g.193122029T>G	GRCh38
NC_000001.10:g.193091159T>G , CM000663.1:g.193091159T>G	GRCh37
NC_000001.9:g.191357782T>G	NCBI36
NG_012691.1:g.5072T>G , LRG_507:g.5072T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000643006.1:c.-172T>G	ENSP00000496633.1:n.-172T>G
ENST00000649895.1:n.47T>G
ENST00000367435.3:c.-172T>G	ENSP00000356405.3:n.-172T>G
NM_024529.4:c.-172T>G , LRG_507t1:c.-172T>G	NP_078805.3:n.-172T>G
XR_001738350.1:n.1628A>C