Canonical Allele Identifier: CA1303232
Gene: CDC73 HGNC NCBI

Linked Data

ClinVar Variation Id: 261739
ClinVar RCV Id: RCV000247723 RCV000271289 RCV000357702 RCV000321566 RCV000590347
dbSNP Id: rs188082584
ExAC: 1:193091321 G / T
gnomAD v2: 1-193091321-G-T
gnomAD v3: 1-193122191-G-T
gnomAD v4: 1-193122191-G-T
MyVariant Identifiers: chr1:g.193091321G>T (hg19) chr1:g.193122191G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122191G>T , CM000663.2:g.193122191G>T GRCh38
NC_000001.10:g.193091321G>T , CM000663.1:g.193091321G>T GRCh37
NC_000001.9:g.191357944G>T NCBI36
NG_012691.1:g.5234G>T , LRG_507:g.5234G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-10G>T MANE Select ENSP00000356405.4:n.-10G>T
ENST00000635846.1:c.-10G>T ENSP00000490035.1:n.-10G>T
ENST00000643006.1:c.-10G>T ENSP00000496633.1:n.-10G>T
ENST00000643784.1:c.-10G>T ENSP00000494944.1:n.-10G>T
ENST00000648071.1:c.-10G>T ENSP00000497513.1:n.-10G>T
ENST00000649606.1:n.4G>T
ENST00000649895.1:n.209G>T
ENST00000650197.1:c.-10G>T ENSP00000496929.1:n.-10G>T
ENST00000367435.3:c.-10G>T ENSP00000356405.3:n.-10G>T
NM_024529.4:c.-10G>T , LRG_507t1:c.-10G>T NP_078805.3:n.-10G>T
XM_006711537.2:c.-10G>T XP_006711600.1:n.-10G>T
XM_006711537.4:c.-10G>T XP_006711600.1:n.-10G>T
XR_001738350.1:n.1466C>A
NM_024529.5:c.-10G>T MANE Select NP_078805.3:n.-10G>T
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