Canonical Allele Identifier: CA2649598765
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103178179
gnomAD v4: 1-193203900-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203900C>A , CM000663.2:g.193203900C>A GRCh38
NC_000001.10:g.193173030C>A , CM000663.1:g.193173030C>A GRCh37
NC_000001.9:g.191439653C>A NCBI36
NG_012691.1:g.86943C>A , LRG_507:g.86943C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.1030+48C>A MANE Select ENSP00000356405.4:n.1030+48C>A
ENST00000635846.1:c.787+48C>A ENSP00000490035.1:n.787+48C>A
ENST00000643006.1:c.1098+48C>A ENSP00000496633.1:n.1098+48C>A
ENST00000648071.1:c.*1006+48C>A ENSP00000497513.1:n.*1006+48C>A
ENST00000649613.1:n.280+48C>A
ENST00000649895.1:n.1248+48C>A
ENST00000650197.1:c.1030+48C>A ENSP00000496929.1:n.1030+48C>A
ENST00000367435.3:c.1030+48C>A ENSP00000356405.3:n.1030+48C>A
NM_024529.4:c.1030+48C>A , LRG_507t1:c.1030+48C>A NP_078805.3:n.1030+48C>A
NM_024529.5:c.1030+48C>A MANE Select NP_078805.3:n.1030+48C>A
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