Canonical Allele Identifier: CA431165604
Gene: XRCC5 HGNC NCBI

Linked Data

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

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

Transcript Alleles

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