Canonical Allele Identifier: CA11137821
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs11685387

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216109091C>T , CM000664.2:g.216109091C>T GRCh38
NC_000002.11:g.216973814C>T , CM000664.1:g.216973814C>T GRCh37
NC_000002.10:g.216682059C>T NCBI36
NG_029780.1:g.4795C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000392133.7:c.-346C>T ENSP00000375978.3:n.-346C>T