Canonical Allele Identifier: CA34407566
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs999627081
gnomAD v3: 1-193122010-G-C
gnomAD v4: 1-193122010-G-C
MyVariant Identifiers: chr1:g.193091140G>C (hg19) chr1:g.193122010G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122010G>C , CM000663.2:g.193122010G>C GRCh38
NC_000001.10:g.193091140G>C , CM000663.1:g.193091140G>C GRCh37
NC_000001.9:g.191357763G>C NCBI36
NG_012691.1:g.5053G>C , LRG_507:g.5053G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000643006.1:c.-191G>C ENSP00000496633.1:n.-191G>C
ENST00000649895.1:n.28G>C
NM_024529.4:c.-191G>C , LRG_507t1:c.-191G>C NP_078805.3:n.-191G>C
XR_001738350.1:n.1647C>G
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