Canonical Allele Identifier: CA34407556
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs973713536
gnomAD v2: 1-193091136-C-T
gnomAD v3: 1-193122006-C-T
gnomAD v4: 1-193122006-C-T
MyVariant Identifiers: chr1:g.193091136C>T (hg19) chr1:g.193122006C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122006C>T , CM000663.2:g.193122006C>T GRCh38
NC_000001.10:g.193091136C>T , CM000663.1:g.193091136C>T GRCh37
NC_000001.9:g.191357759C>T NCBI36
NG_012691.1:g.5049C>T , LRG_507:g.5049C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643006.1:c.-195C>T ENSP00000496633.1:n.-195C>T
ENST00000649895.1:n.24C>T
NM_024529.4:c.-195C>T , LRG_507t1:c.-195C>T NP_078805.3:n.-195C>T
XR_001738350.1:n.1651G>A
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