Canonical Allele Identifier: CA2649624565

Gene: CDC73

Linked Data

• dbSNP Id: rs2103111171
• gnomAD v4: 1-193122044-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122044C>T , CM000663.2:g.193122044C>T	GRCh38
NC_000001.10:g.193091174C>T , CM000663.1:g.193091174C>T	GRCh37
NC_000001.9:g.191357797C>T	NCBI36
NG_012691.1:g.5087C>T , LRG_507:g.5087C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-157C>T MANE Select	ENSP00000356405.4:n.-157C>T
ENST00000643006.1:c.-157C>T	ENSP00000496633.1:n.-157C>T
ENST00000649895.1:n.62C>T
ENST00000367435.3:c.-157C>T	ENSP00000356405.3:n.-157C>T
NM_024529.4:c.-157C>T , LRG_507t1:c.-157C>T	NP_078805.3:n.-157C>T
XM_006711537.2:c.-157C>T	XP_006711600.1:n.-157C>T
XM_006711537.4:c.-157C>T	XP_006711600.1:n.-157C>T
XR_001738350.1:n.1613G>A
NM_024529.5:c.-157C>T MANE Select	NP_078805.3:n.-157C>T