Canonical Allele Identifier: CA2638988398
Gene: RAD51C HGNC NCBI

Linked Data

gnomAD v4: 17-58692435-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692435A>G , CM000679.2:g.58692435A>G GRCh38
NC_000017.10:g.56769796A>G , CM000679.1:g.56769796A>G GRCh37
NC_000017.9:g.54124795A>G NCBI36
NG_023199.1:g.4834A>G , LRG_314:g.4834A>G
NG_047169.1:g.4645T>C

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-209A>G XP_006722064.1:n.-209A>G
XM_006722002.4:c.-209A>G XP_006722065.1:n.-209A>G
XR_934513.3:n.296A>G
XR_934514.3:n.296A>G
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