Canonical Allele Identifier: CA528019114
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1342102599
gnomAD v2: 1-193220973-T-C
gnomAD v3: 1-193251843-T-C
gnomAD v4: 1-193251843-T-C
MyVariant Identifiers: chr1:g.193220973T>C (hg19) chr1:g.193220973_193220974delinsCG (hg19) chr1:g.193251843T>C (hg38) chr1:g.193251843_193251844delinsCG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251843T>C , CM000663.2:g.193251843T>C GRCh38
NC_000001.10:g.193220973T>C , CM000663.1:g.193220973T>C GRCh37
NC_000001.9:g.191487596T>C NCBI36
NG_012691.1:g.134886T>C , LRG_507:g.134886T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1131T>C MANE Select ENSP00000356405.4:n.*1131T>C
ENST00000635846.1:c.*1131T>C ENSP00000490035.1:n.*1131T>C
ENST00000643006.1:c.*1637T>C ENSP00000496633.1:n.*1637T>C
ENST00000367435.3:c.*1131T>C ENSP00000356405.3:n.*1131T>C
NM_024529.4:c.*1131T>C , LRG_507t1:c.*1131T>C NP_078805.3:n.*1131T>C
NM_024529.5:c.*1131T>C MANE Select NP_078805.3:n.*1131T>C
Search 100 bp 5'
Search 100 bp 3'