Canonical Allele Identifier: CA35097856

Gene: CDC73

Linked Data

• dbSNP Id: rs757871416
• gnomAD v2: 1-193172892-T-G
• gnomAD v4: 1-193203762-T-G
• MyVariant Identifiers: chr1:g.193172892T>G (hg19) ; chr1:g.193203762T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203762T>G , CM000663.2:g.193203762T>G	GRCh38
NC_000001.10:g.193172892T>G , CM000663.1:g.193172892T>G	GRCh37
NC_000001.9:g.191439515T>G	NCBI36
NG_012691.1:g.86805T>G , LRG_507:g.86805T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-33T>G MANE Select	ENSP00000356405.4:n.973-33T>G
ENST00000635846.1:c.730-33T>G	ENSP00000490035.1:n.730-33T>G
ENST00000643006.1:c.1041-33T>G	ENSP00000496633.1:n.1041-33T>G
ENST00000648071.1:c.*949-33T>G	ENSP00000497513.1:n.*949-33T>G
ENST00000649613.1:n.223-33T>G
ENST00000649895.1:n.1191-33T>G
ENST00000650197.1:c.973-33T>G	ENSP00000496929.1:n.973-33T>G
ENST00000367435.3:c.973-33T>G	ENSP00000356405.3:n.973-33T>G
NM_024529.4:c.973-33T>G , LRG_507t1:c.973-33T>G	NP_078805.3:n.973-33T>G
NM_024529.5:c.973-33T>G MANE Select	NP_078805.3:n.973-33T>G