Canonical Allele Identifier: CA2649624649
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103111290

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122111G>A , CM000663.2:g.193122111G>A GRCh38
NC_000001.10:g.193091241G>A , CM000663.1:g.193091241G>A GRCh37
NC_000001.9:g.191357864G>A NCBI36
NG_012691.1:g.5154G>A , LRG_507:g.5154G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-90G>A MANE Select ENSP00000356405.4:n.-90G>A
ENST00000643006.1:c.-90G>A ENSP00000496633.1:n.-90G>A
ENST00000649895.1:n.129G>A
ENST00000650197.1:c.-90G>A ENSP00000496929.1:n.-90G>A
ENST00000367435.3:c.-90G>A ENSP00000356405.3:n.-90G>A
NM_024529.4:c.-90G>A , LRG_507t1:c.-90G>A NP_078805.3:n.-90G>A
XM_006711537.2:c.-90G>A XP_006711600.1:n.-90G>A
XM_006711537.4:c.-90G>A XP_006711600.1:n.-90G>A
XR_001738350.1:n.1546C>T
NM_024529.5:c.-90G>A MANE Select NP_078805.3:n.-90G>A