Canonical Allele Identifier: CA2267813897
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2047788318

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692567A>G , CM000679.2:g.58692567A>G GRCh38
NC_000017.10:g.56769928A>G , CM000679.1:g.56769928A>G GRCh37
NC_000017.9:g.54124927A>G NCBI36
NG_023199.1:g.4966A>G , LRG_314:g.4966A>G
NG_047169.1:g.4513T>C

Transcript Alleles

HGVS Amino-acid Change
XM_006722005.2:c.-272A>G XP_006722068.1:n.-272A>G
XM_006722001.4:c.-77A>G XP_006722064.1:n.-77A>G
XM_006722002.4:c.-77A>G XP_006722065.1:n.-77A>G
XM_006722005.3:c.-272A>G XP_006722068.1:n.-272A>G
XM_017024917.1:c.-272A>G XP_016880406.1:n.-272A>G
XR_934513.3:n.428A>G
XR_934514.3:n.428A>G