Canonical Allele Identifier: CA729322952
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1335694573
MyVariant Identifiers: chr1:g.193220572T>G (hg19) chr1:g.193251442T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251442T>G , CM000663.2:g.193251442T>G GRCh38
NC_000001.10:g.193220572T>G , CM000663.1:g.193220572T>G GRCh37
NC_000001.9:g.191487195T>G NCBI36
NG_012691.1:g.134485T>G , LRG_507:g.134485T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*730T>G MANE Select ENSP00000356405.4:n.*730T>G
ENST00000635846.1:c.*730T>G ENSP00000490035.1:n.*730T>G
ENST00000643006.1:c.*1236T>G ENSP00000496633.1:n.*1236T>G
ENST00000367435.3:c.*730T>G ENSP00000356405.3:n.*730T>G
NM_024529.4:c.*730T>G , LRG_507t1:c.*730T>G NP_078805.3:n.*730T>G
NM_024529.5:c.*730T>G MANE Select NP_078805.3:n.*730T>G
Search 100 bp 5'
Search 100 bp 3'