Canonical Allele Identifier: CA773571800
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs1467071020

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692521C>T , CM000679.2:g.58692521C>T GRCh38
NC_000017.10:g.56769882C>T , CM000679.1:g.56769882C>T GRCh37
NC_000017.9:g.54124881C>T NCBI36
NG_023199.1:g.4920C>T , LRG_314:g.4920C>T
NG_047169.1:g.4559G>A

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-123C>T XP_006722064.1:n.-123C>T
XM_006722002.4:c.-123C>T XP_006722065.1:n.-123C>T
XR_934513.3:n.382C>T
XR_934514.3:n.382C>T