Canonical Allele Identifier: CA527707661

Gene: CDC73

Linked Data

• dbSNP Id: rs1363109915
• gnomAD v2: 1-193091171-C-T
• gnomAD v3: 1-193122041-C-T
• gnomAD v4: 1-193122041-C-T
• MyVariant Identifiers: chr1:g.193091171C>T (hg19) ; chr1:g.193122041C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122041C>T , CM000663.2:g.193122041C>T	GRCh38
NC_000001.10:g.193091171C>T , CM000663.1:g.193091171C>T	GRCh37
NC_000001.9:g.191357794C>T	NCBI36
NG_012691.1:g.5084C>T , LRG_507:g.5084C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-160C>T MANE Select	ENSP00000356405.4:n.-160C>T
ENST00000643006.1:c.-160C>T	ENSP00000496633.1:n.-160C>T
ENST00000649895.1:n.59C>T
ENST00000367435.3:c.-160C>T	ENSP00000356405.3:n.-160C>T
NM_024529.4:c.-160C>T , LRG_507t1:c.-160C>T	NP_078805.3:n.-160C>T
XM_006711537.2:c.-160C>T	XP_006711600.1:n.-160C>T
XM_006711537.4:c.-160C>T	XP_006711600.1:n.-160C>T
XR_001738350.1:n.1616G>A
NM_024529.5:c.-160C>T MANE Select	NP_078805.3:n.-160C>T