Canonical Allele Identifier: CA2649624532
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103111110
gnomAD v4: 1-193122017-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122017C>T , CM000663.2:g.193122017C>T GRCh38
NC_000001.10:g.193091147C>T , CM000663.1:g.193091147C>T GRCh37
NC_000001.9:g.191357770C>T NCBI36
NG_012691.1:g.5060C>T , LRG_507:g.5060C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000643006.1:c.-184C>T ENSP00000496633.1:n.-184C>T
ENST00000649895.1:n.35C>T
ENST00000367435.3:c.-184C>T ENSP00000356405.3:n.-184C>T
NM_024529.4:c.-184C>T , LRG_507t1:c.-184C>T NP_078805.3:n.-184C>T
XR_001738350.1:n.1640G>A
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