Canonical Allele Identifier: CA34407722

Gene: CDC73

Linked Data

• dbSNP Id: rs963763476
• gnomAD v2: 1-193091260-A-G
• gnomAD v3: 1-193122130-A-G
• gnomAD v4: 1-193122130-A-G
• MyVariant Identifiers: chr1:g.193091260A>G (hg19) ; chr1:g.193122130A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122130A>G , CM000663.2:g.193122130A>G	GRCh38
NC_000001.10:g.193091260A>G , CM000663.1:g.193091260A>G	GRCh37
NC_000001.9:g.191357883A>G	NCBI36
NG_012691.1:g.5173A>G , LRG_507:g.5173A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-71A>G MANE Select	ENSP00000356405.4:n.-71A>G
ENST00000643006.1:c.-71A>G	ENSP00000496633.1:n.-71A>G
ENST00000643784.1:c.-71A>G	ENSP00000494944.1:n.-71A>G
ENST00000649895.1:n.148A>G
ENST00000650197.1:c.-71A>G	ENSP00000496929.1:n.-71A>G
ENST00000367435.3:c.-71A>G	ENSP00000356405.3:n.-71A>G
NM_024529.4:c.-71A>G , LRG_507t1:c.-71A>G	NP_078805.3:n.-71A>G
XM_006711537.2:c.-71A>G	XP_006711600.1:n.-71A>G
XM_006711537.4:c.-71A>G	XP_006711600.1:n.-71A>G
XR_001738350.1:n.1527T>C
NM_024529.5:c.-71A>G MANE Select	NP_078805.3:n.-71A>G