Canonical Allele Identifier: CA2096681
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs374958902
ExAC: 2:216986743 T / C
gnomAD v2: 2-216986743-T-C
MyVariant Identifiers: chr2:g.216986743T>C (hg19) chr2:g.216122020T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122020T>C , CM000664.2:g.216122020T>C GRCh38
NC_000002.11:g.216986743T>C , CM000664.1:g.216986743T>C GRCh37
NC_000002.10:g.216694988T>C NCBI36
NG_029780.1:g.17724T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.492-42T>C MANE Select ENSP00000375977.2:n.492-42T>C
ENST00000392132.6:c.492-42T>C ENSP00000375977.2:n.492-42T>C
ENST00000392133.7:c.492-42T>C ENSP00000375978.3:n.492-42T>C
ENST00000460284.5:n.1034-42T>C
NM_021141.3:c.492-42T>C NP_066964.1:n.492-42T>C
NM_021141.4:c.492-42T>C MANE Select NP_066964.1:n.492-42T>C
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