Canonical Allele Identifier: CA431165598
Gene: XRCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.216986845C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122122C>A , CM000664.2:g.216122122C>A GRCh38
NC_000002.11:g.216986845C>A , CM000664.1:g.216986845C>A GRCh37
NC_000002.10:g.216695090C>A NCBI36
NG_029780.1:g.17826C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.552C>A MANE Select ENSP00000375977.2:p.Arg184=
ENST00000392132.6:c.552C>A ENSP00000375977.2:p.Arg184=
ENST00000392133.7:c.552C>A ENSP00000375978.3:p.Arg184=
ENST00000460284.5:n.1094C>A
NM_021141.3:c.552C>A NP_066964.1:p.Arg184=
NM_021141.4:c.552C>A MANE Select NP_066964.1:p.Arg184=
Search 100 bp 5'
Search 100 bp 3'