Canonical Allele Identifier: CA1216171193
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1572227700
gnomAD v4: 1-193251863-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251863A>C , CM000663.2:g.193251863A>C GRCh38
NC_000001.10:g.193220993A>C , CM000663.1:g.193220993A>C GRCh37
NC_000001.9:g.191487616A>C NCBI36
NG_012691.1:g.134906A>C , LRG_507:g.134906A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*1151A>C MANE Select ENSP00000356405.4:n.*1151A>C
ENST00000635846.1:c.*1151A>C ENSP00000490035.1:n.*1151A>C
ENST00000643006.1:c.*1657A>C ENSP00000496633.1:n.*1657A>C
ENST00000367435.3:c.*1151A>C ENSP00000356405.3:n.*1151A>C
NM_024529.4:c.*1151A>C , LRG_507t1:c.*1151A>C NP_078805.3:n.*1151A>C
NM_024529.5:c.*1151A>C MANE Select NP_078805.3:n.*1151A>C
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