Canonical Allele Identifier: CA1042299478
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1689929579
gnomAD v3: 2-216205670-A-G
gnomAD v4: 2-216205670-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216205670A>G , CM000664.2:g.216205670A>G GRCh38
NC_000002.11:g.217070393A>G , CM000664.1:g.217070393A>G GRCh37
NC_000002.10:g.216778638A>G NCBI36
NG_029780.1:g.101374A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.*468A>G MANE Select ENSP00000375977.2:n.*468A>G
ENST00000392132.6:c.*468A>G ENSP00000375977.2:n.*468A>G
ENST00000392133.7:c.*468A>G ENSP00000375978.3:n.*468A>G
NM_021141.3:c.*468A>G NP_066964.1:n.*468A>G
NM_021141.4:c.*468A>G MANE Select NP_066964.1:n.*468A>G
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