Canonical Allele Identifier: CA729343958

Gene: CDC73

Linked Data

• dbSNP Id: rs1358174472
• gnomAD v3: 1-193122048-T-C
• gnomAD v4: 1-193122048-T-C
• MyVariant Identifiers: chr1:g.193091178T>C (hg19) ; chr1:g.193122048T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122048T>C , CM000663.2:g.193122048T>C	GRCh38
NC_000001.10:g.193091178T>C , CM000663.1:g.193091178T>C	GRCh37
NC_000001.9:g.191357801T>C	NCBI36
NG_012691.1:g.5091T>C , LRG_507:g.5091T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-153T>C MANE Select	ENSP00000356405.4:n.-153T>C
ENST00000643006.1:c.-153T>C	ENSP00000496633.1:n.-153T>C
ENST00000649895.1:n.66T>C
ENST00000367435.3:c.-153T>C	ENSP00000356405.3:n.-153T>C
NM_024529.4:c.-153T>C , LRG_507t1:c.-153T>C	NP_078805.3:n.-153T>C
XM_006711537.2:c.-153T>C	XP_006711600.1:n.-153T>C
XM_006711537.4:c.-153T>C	XP_006711600.1:n.-153T>C
XR_001738350.1:n.1609A>G
NM_024529.5:c.-153T>C MANE Select	NP_078805.3:n.-153T>C