Canonical Allele Identifier: CA10609149
Gene: CDC73 HGNC NCBI

Linked Data

ClinVar Variation Id: 294421
ClinVar RCV Id: RCV000284170 RCV000341496 RCV000376322
dbSNP Id: rs886045715
MyVariant Identifiers: chr1:g.193220779G>A (hg19) chr1:g.193251649G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251649G>A , CM000663.2:g.193251649G>A GRCh38
NC_000001.10:g.193220779G>A , CM000663.1:g.193220779G>A GRCh37
NC_000001.9:g.191487402G>A NCBI36
NG_012691.1:g.134692G>A , LRG_507:g.134692G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*937G>A MANE Select ENSP00000356405.4:n.*937G>A
ENST00000635846.1:c.*937G>A ENSP00000490035.1:n.*937G>A
ENST00000643006.1:c.*1443G>A ENSP00000496633.1:n.*1443G>A
ENST00000367435.3:c.*937G>A ENSP00000356405.3:n.*937G>A
NM_024529.4:c.*937G>A , LRG_507t1:c.*937G>A NP_078805.3:n.*937G>A
NM_024529.5:c.*937G>A MANE Select NP_078805.3:n.*937G>A
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