Canonical Allele Identifier: CA1042299457
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1689927989
gnomAD v3: 2-216205563-T-G
gnomAD v4: 2-216205563-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216205563T>G , CM000664.2:g.216205563T>G GRCh38
NC_000002.11:g.217070286T>G , CM000664.1:g.217070286T>G GRCh37
NC_000002.10:g.216778531T>G NCBI36
NG_029780.1:g.101267T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.*361T>G MANE Select ENSP00000375977.2:n.*361T>G
ENST00000392132.6:c.*361T>G ENSP00000375977.2:n.*361T>G
ENST00000392133.7:c.*361T>G ENSP00000375978.3:n.*361T>G
NM_021141.3:c.*361T>G NP_066964.1:n.*361T>G
NM_021141.4:c.*361T>G MANE Select NP_066964.1:n.*361T>G
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