Canonical Allele Identifier: CA2638988593
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2047788318
gnomAD v4: 17-58692567-A-C
JSON-LD

Genomic Alleles

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

Transcript Alleles

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