Canonical Allele Identifier: CA2697810987
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103111137
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122031G>A , CM000663.2:g.193122031G>A GRCh38
NC_000001.10:g.193091161G>A , CM000663.1:g.193091161G>A GRCh37
NC_000001.9:g.191357784G>A NCBI36
NG_012691.1:g.5074G>A , LRG_507:g.5074G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-170G>A MANE Select ENSP00000356405.4:n.-170G>A
ENST00000643006.1:c.-170G>A ENSP00000496633.1:n.-170G>A
ENST00000649895.1:n.49G>A
ENST00000367435.3:c.-170G>A ENSP00000356405.3:n.-170G>A
NM_024529.4:c.-170G>A , LRG_507t1:c.-170G>A NP_078805.3:n.-170G>A
XR_001738350.1:n.1626C>T
NM_024529.5:c.-170G>A MANE Select NP_078805.3:n.-170G>A
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