Canonical Allele Identifier: CA2697811661

Gene: CDC73

Linked Data

• dbSNP Id: rs2103111361

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122139G>A , CM000663.2:g.193122139G>A	GRCh38
NC_000001.10:g.193091269G>A , CM000663.1:g.193091269G>A	GRCh37
NC_000001.9:g.191357892G>A	NCBI36
NG_012691.1:g.5182G>A , LRG_507:g.5182G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-62G>A MANE Select	ENSP00000356405.4:n.-62G>A
ENST00000643006.1:c.-62G>A	ENSP00000496633.1:n.-62G>A
ENST00000643784.1:c.-62G>A	ENSP00000494944.1:n.-62G>A
ENST00000649895.1:n.157G>A
ENST00000650197.1:c.-62G>A	ENSP00000496929.1:n.-62G>A
ENST00000367435.3:c.-62G>A	ENSP00000356405.3:n.-62G>A
NM_024529.4:c.-62G>A , LRG_507t1:c.-62G>A	NP_078805.3:n.-62G>A
XM_006711537.2:c.-62G>A	XP_006711600.1:n.-62G>A
XM_006711537.4:c.-62G>A	XP_006711600.1:n.-62G>A
XR_001738350.1:n.1518C>T
NM_024529.5:c.-62G>A MANE Select	NP_078805.3:n.-62G>A