Canonical Allele Identifier: CA2733773034
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2143665785
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692554C>G , CM000679.2:g.58692554C>G GRCh38
NC_000017.10:g.56769915C>G , CM000679.1:g.56769915C>G GRCh37
NC_000017.9:g.54124914C>G NCBI36
NG_023199.1:g.4953C>G , LRG_314:g.4953C>G
NG_047169.1:g.4526G>C

Transcript Alleles

HGVS Amino-acid change
XM_006722005.2:c.-285C>G XP_006722068.1:n.-285C>G
XM_006722001.4:c.-90C>G XP_006722064.1:n.-90C>G
XM_006722002.4:c.-90C>G XP_006722065.1:n.-90C>G
XM_006722005.3:c.-285C>G XP_006722068.1:n.-285C>G
XM_017024917.1:c.-285C>G XP_016880406.1:n.-285C>G
XR_934513.3:n.415C>G
XR_934514.3:n.415C>G
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