Canonical Allele Identifier: CA2697811746
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103111389
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122153C>G , CM000663.2:g.193122153C>G GRCh38
NC_000001.10:g.193091283C>G , CM000663.1:g.193091283C>G GRCh37
NC_000001.9:g.191357906C>G NCBI36
NG_012691.1:g.5196C>G , LRG_507:g.5196C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-48C>G MANE Select ENSP00000356405.4:n.-48C>G
ENST00000643006.1:c.-48C>G ENSP00000496633.1:n.-48C>G
ENST00000643784.1:c.-48C>G ENSP00000494944.1:n.-48C>G
ENST00000649895.1:n.171C>G
ENST00000650197.1:c.-48C>G ENSP00000496929.1:n.-48C>G
ENST00000367435.3:c.-48C>G ENSP00000356405.3:n.-48C>G
NM_024529.4:c.-48C>G , LRG_507t1:c.-48C>G NP_078805.3:n.-48C>G
XM_006711537.2:c.-48C>G XP_006711600.1:n.-48C>G
XM_006711537.4:c.-48C>G XP_006711600.1:n.-48C>G
XR_001738350.1:n.1504G>C
NM_024529.5:c.-48C>G MANE Select NP_078805.3:n.-48C>G
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