Canonical Allele Identifier: CA2697811608

Gene: CDC73

Linked Data

• dbSNP Id: rs2103111335

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122128C>G , CM000663.2:g.193122128C>G	GRCh38
NC_000001.10:g.193091258C>G , CM000663.1:g.193091258C>G	GRCh37
NC_000001.9:g.191357881C>G	NCBI36
NG_012691.1:g.5171C>G , LRG_507:g.5171C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-73C>G MANE Select	ENSP00000356405.4:n.-73C>G
ENST00000643006.1:c.-73C>G	ENSP00000496633.1:n.-73C>G
ENST00000643784.1:c.-73C>G	ENSP00000494944.1:n.-73C>G
ENST00000649895.1:n.146C>G
ENST00000650197.1:c.-73C>G	ENSP00000496929.1:n.-73C>G
ENST00000367435.3:c.-73C>G	ENSP00000356405.3:n.-73C>G
NM_024529.4:c.-73C>G , LRG_507t1:c.-73C>G	NP_078805.3:n.-73C>G
XM_006711537.2:c.-73C>G	XP_006711600.1:n.-73C>G
XM_006711537.4:c.-73C>G	XP_006711600.1:n.-73C>G
XR_001738350.1:n.1529G>C
NM_024529.5:c.-73C>G MANE Select	NP_078805.3:n.-73C>G