Canonical Allele Identifier: CA1303233

Gene: CDC73

Linked Data

• ClinVar Variation Id: 2662681
• ClinVar RCV Id: RCV003441346
• dbSNP Id: rs200382043
• ExAC: 1:193091322 G / C
• gnomAD v2: 1-193091322-G-C
• gnomAD v3: 1-193122192-G-C
• gnomAD v4: 1-193122192-G-C
• MyVariant Identifiers: chr1:g.193091322G>C (hg19) ; chr1:g.193122192G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122192G>C , CM000663.2:g.193122192G>C	GRCh38
NC_000001.10:g.193091322G>C , CM000663.1:g.193091322G>C	GRCh37
NC_000001.9:g.191357945G>C	NCBI36
NG_012691.1:g.5235G>C , LRG_507:g.5235G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-9G>C MANE Select	ENSP00000356405.4:n.-9G>C
ENST00000635846.1:c.-9G>C	ENSP00000490035.1:n.-9G>C
ENST00000643006.1:c.-9G>C	ENSP00000496633.1:n.-9G>C
ENST00000643784.1:c.-9G>C	ENSP00000494944.1:n.-9G>C
ENST00000648071.1:c.-9G>C	ENSP00000497513.1:n.-9G>C
ENST00000649606.1:n.5G>C
ENST00000649895.1:n.210G>C
ENST00000650197.1:c.-9G>C	ENSP00000496929.1:n.-9G>C
ENST00000367435.3:c.-9G>C	ENSP00000356405.3:n.-9G>C
NM_024529.4:c.-9G>C , LRG_507t1:c.-9G>C	NP_078805.3:n.-9G>C
XM_006711537.2:c.-9G>C	XP_006711600.1:n.-9G>C
XM_006711537.4:c.-9G>C	XP_006711600.1:n.-9G>C
XR_001738350.1:n.1465C>G
NM_024529.5:c.-9G>C MANE Select	NP_078805.3:n.-9G>C